Lista de obras - Nila Volpi - Dominio Público Uruguay

A case of amyloid myopathy in a patient with familial Mediterranean fever

artículo científico publicado en 2009

Alternative Pathways of Cancer Cell Death by Rottlerin: Apoptosis versus Autophagy.

artículo científico publicado en 2012

Calf muscle hypertrophy following S1 radiculopathy: A stress disorder caused by hyperactivity with variable response to treatmen

artículo científico publicado en 2018

D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findings

artículo científico publicado en 2010

Endothelin-1 and endothelin-converting enzyme-1 in human granulomatous pathology of eyelid: an immunohistochemical and in situ hybridization study in chalazia.

artículo científico publicado en 2007

Eosinophilia-associated muscle disorders: an immunohistological study with tissue localisation of major basic protein in distinct clinicopathological forms

artículo científico publicado en 2009

Expression of RXFP1 in skin of scleroderma patients and control subjects

artículo científico publicado en 2012

F2-Isoprostanes in soft oral tissues and degree of oral disability after mandibular third molar surgery

artículo científico publicado en 2012

FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation

artículo científico publicado en 2002

Familial multiple exostoses syndrome: a phacomatosis of bone tissue

artículo científico publicado en 1986

Geometric complexity identifies platelet activation in familial hypercholesterolemic patients

artículo científico publicado en 2015

Histopathological findings in systemic sclerosis-related myopathy: fibrosis and microangiopathy with lack of cellular inflammation

artículo científico publicado en 2016

Human osteoarthritic chondrocytes exposed to extremely low-frequency electromagnetic fields (ELF) and therapeutic application of musically modulated electromagnetic fields (TAMMEF) systems: a comparative study.

artículo científico publicado en 2012

Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy

artículo científico publicado en 2017

Is osteopontin involved in cutaneous fibroblast activation? Its hypothetical role in scleroderma pathogenesis

artículo científico publicado en 2014

Lymphatic vessels in human eyelids: an immunohistological study in dermatochalasis and chalazion

scientific article published on 01 March 2008

Lymphatic vessels in human sural nerve: immunohistochemical detection by D2-40

artículo científico publicado en 2006

Muscle mitochondrial changes in cerebrotendinous xanthomatosis

artículo científico publicado en 1991

Next-generation sequencing approach to hyperCKemia: A 2-year cohort study

scientific article published on 16 August 2019

Paraneoplastic necrotizing myopathy associated with adenocarcinoma of the lung - a rare entity with atypical onset: a case report.

artículo científico publicado en 2013

Peptidergic innervation of mesenteric lymphatics in guinea pigs: an immunocytochemical and pharmacological study.

artículo científico publicado en 1991

Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene.

artículo científico publicado en 2011

Rhabdomyolysis in an elderly multitreated patient: multiple drug interactions after statin withdrawal.

artículo científico publicado en 2013

SCN11A variant as possible pain generator in sensory axonal neuropathy

artículo científico publicado en 2019

Sensory-motor axonal multineuropathy during etanercept therapy for rheumatoid arthritis.

artículo científico publicado en 2009

The role of preoperative oxidative stress and mandibular third molar postoperative outcome.

artículo científico publicado en 2013

Two families with novel PMP22 point mutations: genotype-phenotype correlation

scientific article published on 01 September 2009

Uncommon findings in idiopathic hypertrophic cranial pachymeningitis

artículo científico publicado en 2004

Vitamin E deficiency secondary to chronic intestinal malabsorption and effect of vitamin supplement: a case report

artículo científico publicado en 1991

Lista de obras de Nila Volpi

A case of amyloid myopathy in a patient with familial Mediterranean fever

Alternative Pathways of Cancer Cell Death by Rottlerin: Apoptosis versus Autophagy.

Calf muscle hypertrophy following S1 radiculopathy: A stress disorder caused by hyperactivity with variable response to treatmen

D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findings

Endothelin-1 and endothelin-converting enzyme-1 in human granulomatous pathology of eyelid: an immunohistochemical and in situ hybridization study in chalazia.

Eosinophilia-associated muscle disorders: an immunohistological study with tissue localisation of major basic protein in distinct clinicopathological forms

Expression of RXFP1 in skin of scleroderma patients and control subjects

F2-Isoprostanes in soft oral tissues and degree of oral disability after mandibular third molar surgery

FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation

Familial multiple exostoses syndrome: a phacomatosis of bone tissue

Geometric complexity identifies platelet activation in familial hypercholesterolemic patients

Histopathological findings in systemic sclerosis-related myopathy: fibrosis and microangiopathy with lack of cellular inflammation

Human osteoarthritic chondrocytes exposed to extremely low-frequency electromagnetic fields (ELF) and therapeutic application of musically modulated electromagnetic fields (TAMMEF) systems: a comparative study.

Identification and characterization of three novel mutations in the CASQ1 gene in four patients with tubular aggregate myopathy

Is osteopontin involved in cutaneous fibroblast activation? Its hypothetical role in scleroderma pathogenesis

Lymphatic vessels in human eyelids: an immunohistological study in dermatochalasis and chalazion

Lymphatic vessels in human sural nerve: immunohistochemical detection by D2-40

Muscle mitochondrial changes in cerebrotendinous xanthomatosis

Next-generation sequencing approach to hyperCKemia: A 2-year cohort study

Paraneoplastic necrotizing myopathy associated with adenocarcinoma of the lung - a rare entity with atypical onset: a case report.

Peptidergic innervation of mesenteric lymphatics in guinea pigs: an immunocytochemical and pharmacological study.

Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene.

Rhabdomyolysis in an elderly multitreated patient: multiple drug interactions after statin withdrawal.

SCN11A variant as possible pain generator in sensory axonal neuropathy

Sensory-motor axonal multineuropathy during etanercept therapy for rheumatoid arthritis.

The role of preoperative oxidative stress and mandibular third molar postoperative outcome.

Two families with novel PMP22 point mutations: genotype-phenotype correlation

Uncommon findings in idiopathic hypertrophic cranial pachymeningitis

Vitamin E deficiency secondary to chronic intestinal malabsorption and effect of vitamin supplement: a case report