Lista de obras - Christer Holmberg - Dominio Público Uruguay

A missense mutation in SLC26A3 is associated with human male subfertility and impaired activation of CFTR.

artículo científico publicado en 2017

A new tubular disorder with hypokalaemic metabolic alkalosis, severe hypermagnesuric hypomagnesaemia, hypercalciuria and cardiomyopathy

artículo científico publicado en 2005

Adequacy of dialysis with tidal and continuous cycling peritoneal dialysis in children

scientific article published on 01 September 2000

Alphacalcidol oral pulses normalize uremic hyperparathyroidism prior to dialysis

artículo científico publicado en 1995

Apoptotic cell death in human chronic renal allograft rejection

scientific article published on 01 January 1997

Better renal function with enhanced immunosuppression and protocol biopsies after kidney transplantation in children

artículo científico publicado en 2005

COMPARISON OF CONVENTIONAL ORAL CYCLOSPORINE AND CYCLOSPORINE MICROEMULSION FORMULATIONS IN CHILDREN WITH A LIVER TRANSPLANT

artículo científico publicado en 1996

Chronic rejection and late renal allograft dysfunction

artículo científico publicado en 1996

Clinical outcome of pediatric patients on peritoneal dialysis under adequacy control

artículo científico publicado en 2000

Clinical quiz. Congenital nephrotic syndrome, microcephaly, brain malformations and diaphragmatic abnormality associated with histological features of diffuse mesangial sclerosis

artículo científico publicado en 1991

Clustering of private mutations in the congenital chloride diarrhea/down-regulated in adenoma gene

artículo científico publicado en 1998

Clustering of private mutations in the congenital chloride diarrhea/down‐regulated in adenoma gene

article

Congenital nephrosis of the Finnish type (CNF): matrix components of the glomerular basement membranes and of cultured mesangial cells ⬇️

artículo científico publicado el 1 de septiembre de 1993

Congenital nephrotic syndrome

artículo científico publicado en 1996

Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients

artículo científico publicado en 2000

Congenital nephrotic syndrome and recurrence of proteinuria after renal transplantation

artículo científico

Congenital nephrotic syndrome of the Finnish type is not associated with the Pax-2 gene despite the promising transgenic animal model

artículo científico publicado en 1994

Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19

artículo científico publicado en 1994

Conversion from cyclosporine to Neoral in pediatric recipients for kidney, liver, and heart transplantation

scientific article published on 01 August 1996

Course of renal allograft histopathology after transplantation in early childhood

scientific article published on 01 August 2000

Diagnosis and treatment of urinary tract infections in children

artículo científico publicado en 1992

Differences in linear growth and cortisol production between liver and renal transplant recipients on similar immunosuppression

artículo científico publicado en 1995

Disruption of the SLC26A3-mediated anion transport is associated with male subfertility.

artículo científico publicado en 2006

Distinct outcomes of chloride diarrhoea in two siblings with identical genetic background of the disease: implications for early diagnosis and treatment

artículo científico publicado en 2001

Distribution of renal integrin receptors and their ligands in congenital nephrotic syndrome of the Finnish type

scientific article published on 01 August 1996

Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?

artículo científico publicado en 2001

Does acute rejection correlate with infection in liver transplantation?

artículo científico publicado el 1 de febrero de 1992

Early treatment of acute rejections gives favorable long-term function after renal transplantation in small children

artículo científico publicado en 2007

Effect of donor source on renal allograft function in children on triple immunosuppression

scientific article published on 01 January 1994

Exclusion of eight genes as mutated loci in congenital nephrotic syndrome of the Finnish type

artículo científico publicado en 1994

Expression of SLC26A3, CFTR and NHE3 in the human male reproductive tract: role in male subfertility caused by congenital chloride diarrhoea.

artículo científico publicado en 2006

Expression of ion transport-associated proteins in human efferent and epididymal ducts

artículo científico publicado en 2007

Expression of nephrin in pediatric kidney diseases

scientific article published on 01 February 2001

Expression of nine developmental stage-specific genes in human kidney and cultured renal cells

artículo científico publicado en 1997

Factors affecting growth after pediatric liver transplantation

artículo científico publicado en 1994

Feasibility of diagnosing subclinical renal allograft rejection in children by whole blood gene expression analysis

artículo científico publicado en 2008

Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1.

artículo científico publicado en 1995

Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium

artículo científico publicado en 1995

Fine-needle aspiration biopsy allows early detection of acute rejection in children after renal transplantation

artículo científico publicado en 2001

Fine-needle aspiration biopsy in the monitoring of liver allografts. Different cellular findings during rejection and cytomegalovirus infection

artículo científico publicado en 1990

Functional and histopathological cyclosporine A nephrotoxicity in children after organ transplantation

artículo científico publicado en 1995

Ganciclovir in the treatment of severe cytomegalovirus disease in liver transplant patients

artículo científico publicado en 1990

Genetic background of congenital chloride diarrhea in high-incidence populations: Finland, Poland, and Saudi Arabia and Kuwait

artículo científico publicado en 1998

Genetic kidney diseases disclose the pathogenesis of proteinuria

artículo científico publicado en 2001

Genomic structure of the human congenital chloride diarrhea (CLD) gene

artículo científico publicado en 1998

Glomerular anionic charge in congenital nephrotic syndrome of the Finnish type ⬇️

artículo científico publicado el 1 de julio de 1995

Glomerular antigens in severe hereditary nephrosis

artículo científico publicado en 1995

Growth after renal transplantation in infancy or early childhood

artículo científico publicado en 2002

Growth and renal function after liver transplantation in children

artículo científico publicado el 1 de febrero de 1992

Growth delay after liver transplantation in childhood: studies of underlying mechanisms

artículo científico publicado en 1995

Haplotype analysis of congenital nephrotic syndrome of the Finnish type in non-Finnish families

artículo científico publicado en 1996

Headache in children and adolescents after organ transplantation

artículo científico publicado en 2008

High prevalence of asymptomatic vertebral fractures in children after orthotopic liver transplantation

Hypertension, cardiac state, and the role of volume overload during peritoneal dialysis

artículo científico publicado en 2001

Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea

artículo científico publicado en 2001

Improved prenatal diagnosis of the congenital nephrotic syndrome of the Finnish type based on DNA analysis

scientific article published on 01 March 1997

Incidence and predictors of fractures in children after solid organ transplantation: a 5-year prospective, population-based study

artículo científico publicado en 2005

Infections in infants with congenital nephrosis of the Finnish type

artículo científico publicado en 1997

Infections in pediatric kidney and liver transplant patients after perioperative hospitalization

artículo científico publicado en 2000

Influence of pregnancy on kidney graft function

artículo científico publicado en 1993

Is the Finnish heritage of disease disappearing?

artículo científico publicado el 1 de enero de 1992

KIDNEY FUNCTION AFTER 1:1 CONVERSION TO THE CYCLOSPORINE MICROEMULSION FORMULATION IN CHILDREN WITH LIVER ALLOGRAFTS

artículo científico publicado en 1997

Kidney function in cyclosporine-treated pediatric heart transplant recipients

artículo científico publicado en 1997

Kidneys with heavy proteinuria show fibrosis, inflammation, and oxidative stress, but no tubular phenotypic change.

artículo científico publicado en 2005

Liver transplants in Finland: the first 100 patients

artículo científico publicado el 1 de enero de 1992

Long-term changes in cyclosporine pharmacokinetics after renal transplantation in children: evidence for saturable presystemic metabolism and effect of NR1I2 polymorphism

artículo científico publicado en 2010

Long-term clinical outcome in patients with congenital chloride diarrhea

artículo científico publicado en 2006

Long-term effects of paediatric kidney transplantation

artículo científico publicado en 2015

Long-term follow up of renal function and histology after renal allograft transplantation in early childhood

scientific article published on 01 January 1998

Long-term renal function in children after liver transplantation

artículo científico publicado en 2011

Management of congenital nephrotic syndrome of the Finnish type

artículo científico publicado en 1995

Maternal and paternal chromosomes 7 show differential methylation of many genes in lymphoblast DNA.

artículo científico publicado en 2001

Mechanisms and treatment of growth retardation in children with liver transplants

scientific article published on 01 February 1997

Mechanisms of proteinuria: vascular permeability factor in congenital nephrotic syndrome of the Finnish type

scientific article published on 01 November 1996

Methylprednisolone Exposure, Rather than Dose, Predicts Adrenal Suppression and Growth Inhibition in Children with Liver and Renal Transplants1

artículo científico publicado en 1997

Morphologic changes suggesting abnormal renal differentiation in congenital nephrotic syndrome

artículo científico publicado en 1998

Muscular dystonia and athetosis in six patients with congenital nephrotic syndrome of the Finnish type (NPHS1).

artículo científico publicado en 2005

Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea

artículo científico publicado en 1996

Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS).

artículo científico publicado en 2004

Nephrin is specifically located at the slit diaphragm of glomerular podocytes

artículo científico publicado en 1999

Neurocognitive function of pediatric heart transplant recipients.

artículo científico publicado en 2010

Neurodevelopmental outcome in high-risk patients after renal transplantation in early childhood

artículo científico publicado en 2002

Neurological development in 21 children on peritoneal dialysis in infancy

artículo científico publicado en 2011

Neuropsychological profile of children with kidney transplants

artículo científico publicado en 2011

Neuroradiologic findings in children with renal transplantation under 5 years of age.

artículo científico publicado en 2004

Noncollagenous matrix components of glomeruli in congenital nephrotic syndrome of the Finnish type: evidence of abnormal splitting of nidogen?

artículo científico publicado en 1996

Normal growth and intravascular volume status with good metabolic control during peritoneal dialysis in infancy

artículo científico publicado en 2010

Oral butyrate in treatment of congenital chloride diarrhea

artículo científico publicado en 2008

Organ transplantation in children.

artículo científico publicado en 1997

Paediatric kidney transplantation

artículo científico publicado en 1998

Parent-child and spousal relationships in families with a young child with end-stage renal disease

artículo científico publicado en 2013

Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea.

artículo científico publicado en 1994

Pediatric organ transplantation in Finland

artículo científico publicado el 1 de enero de 1992

Peritoneal dialysis in children under 5 years of age

artículo científico publicado en 1997

Pharmacogenetics of cyclosporine in children suggests an age-dependent influence of ABCB1 polymorphisms

artículo científico publicado en 2008

Pharmacokinetically determined cyclosporine dosage in young children

artículo científico publicado en 1991

Pharmacokinetics and pharmacodynamics of pravastatin in pediatric and adolescent cardiac transplant recipients on a regimen of triple immunosuppression

artículo científico publicado en 2004

Pharmacokinetics and response to pravastatin in paediatric patients with familial hypercholesterolaemia and in paediatric cardiac transplant recipients in relation to polymorphisms of the SLCO1B1 and ABCB1 genes

artículo científico publicado en 2006

Podocytes are firmly attached to glomerular basement membrane in kidneys with heavy proteinuria

artículo científico publicado en 2004

Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31

article

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

artículo científico publicado en 1998

Post-transplantation nephrosis in congenital nephrotic syndrome of the Finnish type.

artículo científico publicado en 1993

Predictive value of pretransplantation cyclosporine pharmacokinetic studies on initial post-transplantation dosing in pediatric kidney allograft recipients

artículo científico publicado en 2003

Proteinuria and prenatal diagnosis of congenital nephrosis in fetal carriers of nephrin gene mutations

artículo científico publicado en 2002

Psychosocial adaptation after solid organ transplantation in children

artículo científico publicado en 2003

Psychosocial adjustment and quality of life after renal transplantation in early childhood.

artículo científico publicado en 2004

Quality of life in adult survivors of pediatric kidney transplantation

artículo científico publicado en 2011

Recombinant human growth hormone improves growth in children receiving glucocorticoid treatment after liver transplantation

artículo científico publicado en 1996

Recombinant human growth hormone treatment. Its effect on renal allograft function and histology.

artículo científico publicado en 1996

Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type: role of nephrin.

artículo científico publicado en 2002

Renal allograft function and histology in children on triple immunosuppression based on individual pharmacokinetically determined cyclosporine administration

artículo científico publicado en 1994

Renal allograft histology and correlation with function in children on triple therapy

artículo científico publicado en 1995

Renal function and histopathologic changes in children after liver transplantation

scientific article published on 01 December 1994

Renal transplantation and parenthood

artículo científico publicado el 1 de octubre de 1992

Renal transplantation in children under 5 years of age

artículo científico publicado en 1994

Renal transplantation in children with congenital nephrotic syndrome of the Finnish type

artículo científico publicado en 1990

Renal transplantation in children with emphasis on young patients

artículo científico publicado en 1994

Renal transplantation in infants

artículo científico

Renal transplantation in small children with congenital nephrotic syndrome of the Finnish type.

artículo científico publicado en 1991

Resistance to activated protein C as an underlying cause of recurrent venous thrombosis during relapsing nephrotic syndrome ⬇️

artículo científico publicado el 1 de julio de 1995

Review article: the clinical management of congenital chloride diarrhoea

artículo científico publicado en 2009

Risk factors for impaired quality of life and psychosocial adjustment after pediatric heart, kidney, and liver transplantation

artículo científico publicado en 2013

Role of nephrin in cell junction formation in human nephrogenesis

artículo científico publicado en 2000

SLC26A3 mutations in congenital chloride diarrhea

artículo científico publicado en 2002

Serum C-reactive protein in pediatric kidney and liver transplant patients

artículo científico publicado en 2002

Sphingolipid activator proteins in a human hereditary renal disease with deposition of disialogangliosides

artículo científico publicado en 1996

Spine after solid organ transplantation in childhood: a clinical, radiographic, and magnetic resonance imaging analysis of 40 patients

artículo científico publicado en 2006

Successful liver transplantation after induction chemotherapy in children with inoperable, multifocal primary hepatic malignancy.

artículo científico publicado en 1999

Surgical correction of spinal deformities after solid organ transplantation in childhood

artículo científico publicado en 2006

The Nephropathy of Type I Tyrosinemia after Liver Transplantation ⬇️

artículo científico publicado el 1 de mayo de 1995

The congenital chloride diarrhea gene is expressed in seminal vesicle, sweat gland, inflammatory colon epithelium, and in some dysplastic colon cells

article

The gene for congenital chloride diarrhea maps close to but is distinct from the gene for cystic fibrosis transmembrane conductance regulator

artículo científico publicado en 1993

The glycosaminoglycan content of renal basement membranes in the congenital nephrotic syndrome of the Finnish type

artículo científico publicado el 1 de enero de 1992

The impact of sodium chloride and volume depletion in the chronic kidney disease of congenital chloride diarrhea

article by Satu Wedenoja et al published October 2008 in Kidney International

The number of podocyte slit diaphragms is decreased in minimal change nephrotic syndrome.

artículo científico publicado en 2002

The use of fine-needle aspiration biopsy in detection of acute rejection in children after liver transplantation

artículo científico publicado en 2002

Therapy insight: orthopedic complications after solid organ transplantation in childhood

artículo científico publicado en 2007

Thirty years of renal transplantation in Helsinki

artículo científico publicado en 1994

Tissue expression of nephrin in human and pig.

artículo científico publicado en 2004

Tubular effects of cyclosporine in pediatric renal transplant recipients

artículo científico publicado en 1996

Update on SLC26A3 mutations in congenital chloride diarrhea

artículo científico publicado en 2011

Visuospatial impairment in children and adolescents after liver transplantation ⬇️

artículo científico publicado el 29 de diciembre de 2010

[Function of the kidney II: tubule and collecting tubule]

artículo científico publicado en 1998

[Organ transplantation in children is a rational therapy]

scientific article published on 01 January 1995

[Severe kidney diseases in children]

artículo científico publicado en 1997

Lista de obras de Christer Holmberg

A missense mutation in SLC26A3 is associated with human male subfertility and impaired activation of CFTR.

A new tubular disorder with hypokalaemic metabolic alkalosis, severe hypermagnesuric hypomagnesaemia, hypercalciuria and cardiomyopathy

Adequacy of dialysis with tidal and continuous cycling peritoneal dialysis in children

Alphacalcidol oral pulses normalize uremic hyperparathyroidism prior to dialysis

Apoptotic cell death in human chronic renal allograft rejection

Better renal function with enhanced immunosuppression and protocol biopsies after kidney transplantation in children

COMPARISON OF CONVENTIONAL ORAL CYCLOSPORINE AND CYCLOSPORINE MICROEMULSION FORMULATIONS IN CHILDREN WITH A LIVER TRANSPLANT

Chronic rejection and late renal allograft dysfunction

Clinical outcome of pediatric patients on peritoneal dialysis under adequacy control

Clinical quiz. Congenital nephrotic syndrome, microcephaly, brain malformations and diaphragmatic abnormality associated with histological features of diffuse mesangial sclerosis

Clustering of private mutations in the congenital chloride diarrhea/down-regulated in adenoma gene

Clustering of private mutations in the congenital chloride diarrhea/down‐regulated in adenoma gene

Congenital nephrosis of the Finnish type (CNF): matrix components of the glomerular basement membranes and of cultured mesangial cells ⬇️

Congenital nephrotic syndrome

Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients

Congenital nephrotic syndrome and recurrence of proteinuria after renal transplantation

Congenital nephrotic syndrome of the Finnish type is not associated with the Pax-2 gene despite the promising transgenic animal model

Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19

Conversion from cyclosporine to Neoral in pediatric recipients for kidney, liver, and heart transplantation

Course of renal allograft histopathology after transplantation in early childhood

Diagnosis and treatment of urinary tract infections in children

Differences in linear growth and cortisol production between liver and renal transplant recipients on similar immunosuppression

Disruption of the SLC26A3-mediated anion transport is associated with male subfertility.

Distinct outcomes of chloride diarrhoea in two siblings with identical genetic background of the disease: implications for early diagnosis and treatment

Distribution of renal integrin receptors and their ligands in congenital nephrotic syndrome of the Finnish type

Do patients with maternal uniparental disomy for chromosome 7 have a distinct mild Silver-Russell phenotype?

Does acute rejection correlate with infection in liver transplantation?

Early treatment of acute rejections gives favorable long-term function after renal transplantation in small children

Effect of donor source on renal allograft function in children on triple immunosuppression

Exclusion of eight genes as mutated loci in congenital nephrotic syndrome of the Finnish type

Expression of SLC26A3, CFTR and NHE3 in the human male reproductive tract: role in male subfertility caused by congenital chloride diarrhoea.

Expression of ion transport-associated proteins in human efferent and epididymal ducts

Expression of nephrin in pediatric kidney diseases

Expression of nine developmental stage-specific genes in human kidney and cultured renal cells

Factors affecting growth after pediatric liver transplantation

Feasibility of diagnosing subclinical renal allograft rejection in children by whole blood gene expression analysis

Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1.

Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium

Fine-needle aspiration biopsy allows early detection of acute rejection in children after renal transplantation

Fine-needle aspiration biopsy in the monitoring of liver allografts. Different cellular findings during rejection and cytomegalovirus infection

Functional and histopathological cyclosporine A nephrotoxicity in children after organ transplantation

Ganciclovir in the treatment of severe cytomegalovirus disease in liver transplant patients

Genetic background of congenital chloride diarrhea in high-incidence populations: Finland, Poland, and Saudi Arabia and Kuwait

Genetic kidney diseases disclose the pathogenesis of proteinuria

Genomic structure of the human congenital chloride diarrhea (CLD) gene

Glomerular anionic charge in congenital nephrotic syndrome of the Finnish type ⬇️

Glomerular antigens in severe hereditary nephrosis

Growth after renal transplantation in infancy or early childhood

Growth and renal function after liver transplantation in children

Growth delay after liver transplantation in childhood: studies of underlying mechanisms

Haplotype analysis of congenital nephrotic syndrome of the Finnish type in non-Finnish families

Headache in children and adolescents after organ transplantation

High prevalence of asymptomatic vertebral fractures in children after orthotopic liver transplantation

Hypertension, cardiac state, and the role of volume overload during peritoneal dialysis

Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea

Improved prenatal diagnosis of the congenital nephrotic syndrome of the Finnish type based on DNA analysis

Incidence and predictors of fractures in children after solid organ transplantation: a 5-year prospective, population-based study

Infections in infants with congenital nephrosis of the Finnish type

Infections in pediatric kidney and liver transplant patients after perioperative hospitalization

Influence of pregnancy on kidney graft function

Is the Finnish heritage of disease disappearing?

KIDNEY FUNCTION AFTER 1:1 CONVERSION TO THE CYCLOSPORINE MICROEMULSION FORMULATION IN CHILDREN WITH LIVER ALLOGRAFTS

Kidney function in cyclosporine-treated pediatric heart transplant recipients

Kidneys with heavy proteinuria show fibrosis, inflammation, and oxidative stress, but no tubular phenotypic change.

Liver transplants in Finland: the first 100 patients

Long-term changes in cyclosporine pharmacokinetics after renal transplantation in children: evidence for saturable presystemic metabolism and effect of NR1I2 polymorphism

Long-term clinical outcome in patients with congenital chloride diarrhea

Long-term effects of paediatric kidney transplantation

Long-term follow up of renal function and histology after renal allograft transplantation in early childhood

Long-term renal function in children after liver transplantation

Management of congenital nephrotic syndrome of the Finnish type

Maternal and paternal chromosomes 7 show differential methylation of many genes in lymphoblast DNA.

Mechanisms and treatment of growth retardation in children with liver transplants

Mechanisms of proteinuria: vascular permeability factor in congenital nephrotic syndrome of the Finnish type

Methylprednisolone Exposure, Rather than Dose, Predicts Adrenal Suppression and Growth Inhibition in Children with Liver and Renal Transplants1

Morphologic changes suggesting abnormal renal differentiation in congenital nephrotic syndrome

Muscular dystonia and athetosis in six patients with congenital nephrotic syndrome of the Finnish type (NPHS1).

Mutations of the Down-regulated in adenoma (DRA) gene cause congenital chloride diarrhoea

Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS).