Lista de obras - A Nanda - Dominio Público Uruguay

'Progressive erythematous papules and plaques in an infant: Sweet that is not so sweet!': reply from authors

scientific article published on 31 July 2019

A newborn with a congenital ulcerated plaque on the abdomen

artículo científico publicado en 2020

A prospective survey of pediatric dermatology clinic patients in Kuwait: an analysis of 10,000 cases

artículo científico publicado en 1999

A survey of childhood psoriasis in Kuwait

scientific article published on 01 June 1994

Alopecia and hypotrichosis as characteristic findings in Woodhouse-Sakati syndrome: report of a family with mutation in the C2orf37 gene

artículo científico publicado en 2013

Alopecia areata in children: a clinical profile

artículo científico publicado en 2002

Alopecia in children

artículo científico publicado en 2000

An infant with congenital indurated hairy plaque

scientific article published on 01 September 2011

Anterior cervical hypertrichosis (hairy throat): is it a sign to worry about?

scientific article published on 27 September 2006

Association of linear IgA bullous disease of childhood with Crohn's disease

artículo científico publicado en 2006

Autoimmune diseases associated with neurofibromatosis type 1

artículo científico publicado en 2008

CEDNIK syndrome with phenotypic variability

artículo científico publicado en 2022

Childhood lichen planus: a report of 23 cases

artículo científico publicado en 2001

Childhood psoriasis: an epidemiologic survey of 112 patients

artículo científico publicado en 1990

Chronic cutaneous graft-versus-host disease in children: A report of 14 patients from a tertiary care pediatric dermatology clinic

artículo científico publicado en 2018

Clinical subtypes and molecular basis of epidermolysis bullosa in Kuwait

artículo científico publicado en 2018

Clinicoepidemiological features of mycosis fungoides in Kuwait, 1991–2006 ⬇️

artículo científico publicado el 1 de diciembre de 2010

Clinicopathological features and HLA tissue typing in pemphigoid gestationis patients in Kuwait.

artículo científico publicado en 2003

Coexistence of pemphigus vulgaris with systemic lupus erythematosus

artículo científico publicado en 2004

Concomitance of psoriasis and atopic dermatitis

artículo científico publicado en 1995

Concurrent appearance of alopecia areata in siblings

artículo científico publicado en 1995

Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3

artículo científico publicado en 2017

Congenital linear psoriasis: a case report

artículo científico publicado en 1990

Congenital papulonodular eruption: presenting sign of congenital leukaemia cutis

artículo científico publicado en 2012

Congenital yellow nail syndrome: a case report and its relationship to nonimmune fetal hydrops

artículo científico publicado en 2010

Consanguinity and Double Recessive Gene Pathology: Cutis Laxa (PYCR1) and Nephrotic Syndrome (PLCE1)

scientific article published on 01 February 2019

Cutaneous Lupus Erythematosus in Children: Experience from a Tertiary Care Pediatric Dermatology Clinic

artículo científico publicado en 2016

Dermatological manifestations of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis (POIKTMP): a case series of 28 patients

scientific article published on 10 April 2019

Dermatophytosis of children in Kuwait

artículo científico publicado en 1992

Dermatophytosis of children in Kuwait: a prospective survey

artículo científico publicado en 1993

Dorfman-Chanarin syndrome

artículo científico publicado en 1990

Drug-induced toxic epidermal necrolysis in developing countries

scientific article published on 01 January 1990

Ehlers- Danlos Syndrome

scientific article published on 01 September 1989

Extensive Bilateral Symmetrical Fixed Drug Eruption

scientific article published on 01 July 1989

Extensive postzygotic mosaicism for a novel keratin 10 mutation in epidermolytic ichthyosis

artículo científico publicado en 2014

Familial inflammatory linear verrucous epidermal nevus (ILVEN)

artículo científico publicado en 1994

Febrile ulceronecrotic Mucha-Habermann disease (pityriasis lichenoides et varioliformis acuta fulminans) associated with parvovirus infection.

artículo científico publicado en 2013

Fetal hydantoin syndrome?

scientific article published on 01 March 1989

Fixed drug eruption at the site of BCG vaccination

artículo científico publicado en 1988

Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait.

artículo científico publicado en 2014

Further characterization of ATP6V0A2-related autosomal recessive cutis laxa

artículo científico publicado en 2012

Genetic analysis of interleukin-1 receptor antagonist and interleukin-1β single-nucleotide polymorphisms C-511T and C+3953T in alopecia areata: susceptibility and severity association.

artículo científico publicado en 2013

Genetic evidence for the involvement of NOTCH4 in rheumatoid arthritis and alopecia areata.

artículo científico publicado en 2013

Gerodermia osteodysplastica/wrinkly skin syndrome: Report of three patients and brief review of the literature

artículo científico publicado en 2008

Hair discoloration caused by etretinate

artículo científico publicado en 1994

Homozygous mutations in the 5' region of the JUP gene result in cutaneous disease but normal heart development in children

artículo científico publicado en 2010

Identical glycine substitution mutations in type VII collagen may underlie both dominant and recessive forms of dystrophic epidermolysis bullosa.

artículo científico publicado en 2011

Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes.

artículo científico publicado en 2015

Impact of next generation sequencing on diagnostics in a genetic skin disease clinic

artículo científico publicado en 2013

Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2.

artículo científico publicado en 2007

Incontinentia pigmenti in a father and daughter.

artículo científico publicado en 2016

Ketoconazole in the treatment of cutaneous leishmaniasis in Kuwait

artículo científico publicado en 1995

Keutel syndrome with overlapping features of cutis laxa: A new variant [3]

artículo científico publicado en 2006

Kyrle's disease in a patient with chronic renal failure

artículo científico publicado en 1989

Large Intragenic Deletion in DSTYK Underlies Autosomal-Recessive Complicated Spastic Paraparesis, SPG23.

artículo científico publicado en 2017

Linear IgA bullous disease of childhood: an experience from Kuwait

scientific article published on 01 September 2006

Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1).

artículo científico publicado en 2002

Lipoid proteinosis: Report of four siblings and brief review of the literature

artículo científico publicado en 2001

Lipoid proteinosis: a follow-up comment

artículo científico publicado en 2002

Milia en plaque: a new site

artículo científico publicado en 2000

Multiple milia in a newborn with congenital malformations: oral-facial-digital syndrome type 1.

artículo científico publicado en 2010

Mutations in GRHL2 result in an autosomal-recessive ectodermal Dysplasia syndrome

artículo científico publicado en 2014

Mutations in PYCR1 cause cutis laxa with progeroid features

artículo científico publicado en 2009

Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis

artículo científico publicado en 2003

Mycosis Fungoides in Arab Children and Adolescents: A Report of 36 Patients from Kuwait ⬇️

artículo científico publicado el 1 de noviembre de 2010

Neutrophilic Panniculitis in a child with MYSM1 deficiency

scientific article published on 12 February 2019

Next generation diagnostics of heritable connective tissue disorders

artículo científico publicado en 2014

Noninfectious cutaneous granulomas in primary immunodeficiency disorders: report from a national registry.

artículo científico publicado en 2014

Novel TGM5 mutations in acral peeling skin syndrome.

artículo científico publicado en 2015

Pemphigus in Kuwait

artículo científico publicado en 1999

Pemphigus in pregnancy

scientific article published on 01 October 1989

Phacomatosis pigmentovascularis: Report of four new cases

scientific article published on 01 May 2016

Pityriasis (tinea) versicolor in infancy.

artículo científico publicado en 1988

Progressive erythematous papules and plaques in an infant

scientific article published on 29 May 2019

Rothmund-Thomson syndrome in two siblings.

artículo científico publicado en 1989

Salient features and HLA markers of childhood psoriasis in Kuwait

scientific article published on 01 March 2000

Self-healing juvenile cutaneous mucinosis manifesting with subcutaneous nodules

artículo científico publicado en 2010

Skin manifestations in primary immunodeficient children

artículo científico publicado en 2011

Spectrum of autoimmune bullous diseases among children in Kuwait

artículo científico publicado en 2020

Spectrum of autoimmune bullous diseases in Kuwait

scientific article published on 01 December 2004

Spectrum of cutaneous manifestations among patients with GATA2 deficiency

artículo científico publicado en 2018

Survey of cutaneous lesions in Indian newborns

scientific article published on 01 March 1989

Susceptible and protective endothelial nitric oxide synthase gene polymorphism in alopecia areata in the Kuwaiti population.

artículo científico publicado en 2008

Sweet's syndrome (acute febrile neutrophilic dermatosis) associated with adenocarcinoma of prostate and transitional cell carcinoma of urinary bladder

scientific article published on 01 September 2005

Syndromic inherited poikiloderma due to a de novo mutation in FAM111B.

artículo científico publicado en 2016

Systematised naevus sebaceus resulting from post-zygotic mutation in HRAS

artículo científico publicado en 2015

Temporal case clustering in pityriasis rosea: a regression analysis on 1379 patients in Minnesota, kuwait, and diyarbakir, Turkey

artículo científico publicado en 2005

Thyroid function, autoantibodies, and HLA tissue typing in children with alopecia areata

artículo científico publicado en 2002

Type 2 segmental Hailey-Hailey disease with systematized bilateral arrangement.

artículo científico publicado en 2013

UVB phototherapy in childhood psoriasis

scientific article published on 01 March 1995

Unilesional (segmental) mycosis fungoides presenting in childhood

artículo científico publicado en 2004

What syndrome is this? Autosomal recessive type II cutis laxa

artículo científico publicado en 2004

Whole-exome sequencing diagnosis of two autosomal recessive disorders in one family

artículo científico publicado en 2015

Xanthoma disseminatum

artículo científico publicado en 1990

Lista de obras de A Nanda

'Progressive erythematous papules and plaques in an infant: Sweet that is not so sweet!': reply from authors

A newborn with a congenital ulcerated plaque on the abdomen

A prospective survey of pediatric dermatology clinic patients in Kuwait: an analysis of 10,000 cases

A survey of childhood psoriasis in Kuwait

Alopecia and hypotrichosis as characteristic findings in Woodhouse-Sakati syndrome: report of a family with mutation in the C2orf37 gene

Alopecia areata in children: a clinical profile

Alopecia in children

An infant with congenital indurated hairy plaque

Anterior cervical hypertrichosis (hairy throat): is it a sign to worry about?

Association of linear IgA bullous disease of childhood with Crohn's disease

Autoimmune diseases associated with neurofibromatosis type 1

CEDNIK syndrome with phenotypic variability

Childhood lichen planus: a report of 23 cases

Childhood psoriasis: an epidemiologic survey of 112 patients

Chronic cutaneous graft-versus-host disease in children: A report of 14 patients from a tertiary care pediatric dermatology clinic

Clinical subtypes and molecular basis of epidermolysis bullosa in Kuwait

Clinicoepidemiological features of mycosis fungoides in Kuwait, 1991–2006 ⬇️

Clinicopathological features and HLA tissue typing in pemphigoid gestationis patients in Kuwait.

Coexistence of pemphigus vulgaris with systemic lupus erythematosus

Concomitance of psoriasis and atopic dermatitis

Concurrent appearance of alopecia areata in siblings

Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3

Congenital linear psoriasis: a case report

Congenital papulonodular eruption: presenting sign of congenital leukaemia cutis

Congenital yellow nail syndrome: a case report and its relationship to nonimmune fetal hydrops

Consanguinity and Double Recessive Gene Pathology: Cutis Laxa (PYCR1) and Nephrotic Syndrome (PLCE1)

Cutaneous Lupus Erythematosus in Children: Experience from a Tertiary Care Pediatric Dermatology Clinic

Dermatological manifestations of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis (POIKTMP): a case series of 28 patients

Dermatophytosis of children in Kuwait

Dermatophytosis of children in Kuwait: a prospective survey

Dorfman-Chanarin syndrome

Drug-induced toxic epidermal necrolysis in developing countries

Ehlers- Danlos Syndrome

Extensive Bilateral Symmetrical Fixed Drug Eruption

Extensive postzygotic mosaicism for a novel keratin 10 mutation in epidermolytic ichthyosis

Familial inflammatory linear verrucous epidermal nevus (ILVEN)

Febrile ulceronecrotic Mucha-Habermann disease (pityriasis lichenoides et varioliformis acuta fulminans) associated with parvovirus infection.

Fetal hydantoin syndrome?

Fixed drug eruption at the site of BCG vaccination

Founder mutation in dystonin-e underlying autosomal recessive epidermolysis bullosa simplex in Kuwait.

Further characterization of ATP6V0A2-related autosomal recessive cutis laxa

Genetic analysis of interleukin-1 receptor antagonist and interleukin-1β single-nucleotide polymorphisms C-511T and C+3953T in alopecia areata: susceptibility and severity association.

Genetic evidence for the involvement of NOTCH4 in rheumatoid arthritis and alopecia areata.

Gerodermia osteodysplastica/wrinkly skin syndrome: Report of three patients and brief review of the literature

Hair discoloration caused by etretinate

Homozygous mutations in the 5' region of the JUP gene result in cutaneous disease but normal heart development in children

Identical glycine substitution mutations in type VII collagen may underlie both dominant and recessive forms of dystrophic epidermolysis bullosa.

Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes.

Impact of next generation sequencing on diagnostics in a genetic skin disease clinic

Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2.

Incontinentia pigmenti in a father and daughter.

Ketoconazole in the treatment of cutaneous leishmaniasis in Kuwait

Keutel syndrome with overlapping features of cutis laxa: A new variant [3]

Kyrle's disease in a patient with chronic renal failure

Large Intragenic Deletion in DSTYK Underlies Autosomal-Recessive Complicated Spastic Paraparesis, SPG23.

Linear IgA bullous disease of childhood: an experience from Kuwait

Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1).

Lipoid proteinosis: Report of four siblings and brief review of the literature

Lipoid proteinosis: a follow-up comment

Milia en plaque: a new site

Multiple milia in a newborn with congenital malformations: oral-facial-digital syndrome type 1.

Mutations in GRHL2 result in an autosomal-recessive ectodermal Dysplasia syndrome

Mutations in PYCR1 cause cutis laxa with progeroid features

Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis

Mycosis Fungoides in Arab Children and Adolescents: A Report of 36 Patients from Kuwait ⬇️

Neutrophilic Panniculitis in a child with MYSM1 deficiency

Next generation diagnostics of heritable connective tissue disorders

Noninfectious cutaneous granulomas in primary immunodeficiency disorders: report from a national registry.

Novel TGM5 mutations in acral peeling skin syndrome.

Pemphigus in Kuwait

Pemphigus in pregnancy

Phacomatosis pigmentovascularis: Report of four new cases

Pityriasis (tinea) versicolor in infancy.

Progressive erythematous papules and plaques in an infant

Rothmund-Thomson syndrome in two siblings.

Salient features and HLA markers of childhood psoriasis in Kuwait

Self-healing juvenile cutaneous mucinosis manifesting with subcutaneous nodules

Skin manifestations in primary immunodeficient children

Spectrum of autoimmune bullous diseases among children in Kuwait