Aetiopathology and genetic basis of neonatal diabetes. - Wikidata - awgldk - TriplyDB

Aetiopathology and genetic basis of neonatal diabetes.

Aetiopathology and genetic basis of neonatal diabetes.

http://www.wikidata.org/entity/Q35285260

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Mutations in PTF1A cause pancreatic and cerebellar agenesis Impaired glucose homeostasis in transgenic mice expressing the human transient neonatal diabetes mellitus locus, TNDM Genetics and pathophysiology of neonatal diabetes mellitus.Syndromal obesity due to paternal duplication 6(q24.3-q27).Neonatal diabetes mellitus due to pancreas agenesis: a new case report and review of the literature.A 'picturesque' case of transition from subcutaneous to oral treatment in neonatal diabetes The Missing lnc(RNA) between the pancreatic β-cell and diabetes Deciphering a molecular mechanism of neonatal diabetes mellitus by the chemical synthesis of a protein diastereomer, [D-AlaB8]human proinsulin.Partial paternal uniparental disomy of chromosome 6 in an infant with neonatal diabetes, macroglossia, and craniofacial abnormalities.Genomic imprinting in diabetes.Medical care from childhood to adulthood in type 1 and type 2 diabetes.Transient neonatal diabetes, a disorder of imprinting.Permanent neonatal diabetes mellitus: clinical presentation and epidemiology in Oman.An assessment of pancreatic endocrine function and insulin sensitivity in patients with transient neonatal diabetes in remission Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR3000 (approximately 5.4 Mb) interval on chromosome 6q.Neonatal diabetes mellitus: a disease linked to multiple mechanisms.Insulin gene mutations as a cause of permanent neonatal diabetes.Neonatal diabetes mellitus and congenital diaphragmatic hernia: coincidence or concurrent etiology?Minimal incidence of neonatal/infancy onset diabetes in Italy is 1:90,000 live births Neonatal diabetes mellitus.Current understanding of K ATP channels in neonatal diseases: focus on insulin secretion disorders.The role of pancreatic imaging in monogenic diabetes mellitus.Neonatal diabetes mellitus in China: a case report and review of the Chinese literature.Multilocus methylation defects in imprinting disorders.Role of DNA methylation in imprinting disorders: an updated review.Transient neonatal diabetes mellitus in an extremely preterm infant.Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births.Transient neonatal diabetes mellitus, type 4, type 1 diabetes mellitus, or MODY: which disease is it, anyway?Neonatal diabetes with hyperchylomicronemia.Glibenclamide unresponsiveness in a Brazilian child with permanent neonatal diabetes mellitus and DEND syndrome due to a C166Y mutation in KCNJ11 (Kir6.2) gene.Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia.[Neonatal diabetes mellitus].Transient Neonatal Diabetes due to a Mutation in KCNJ11 in a Child with Klinefelter Syndrome.Neonatal diabetes mellitus: Insulin pump as an alternative management strategy.Successful treatment of young infants presenting neonatal diabetes mellitus with continuous subcutaneous insulin infusion before genetic diagnosis.Continuous subcutaneous insulin infusion in neonatal diabetes mellitus.Permanent neonatal diabetes with arthrogryposis multiplex congenita and neurogenic bladder - a new syndrome?Duplication 6q21q23 in two unrelated patients.A further example of a distinctive autosomal recessive syndrome comprising neonatal diabetes mellitus, intestinal atresias and gall bladder agenesis.Permanent neonatal diabetes caused by a novel mutation.

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P2860

Aetiopathology and genetic basis of neonatal diabetes.

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1997 թուականի Յունուարին հրատարակուած գիտական յօդուած

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Aetiopathology and genetic basis of neonatal diabetes.

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Aetiopathology and genetic basis of neonatal diabetes.

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Aetiopathology and genetic basis of neonatal diabetes.

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Archives of Disease in Childhood. Fetal and Neonatal Edition

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Aetiopathology and genetic basis of neonatal diabetes.

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D O Robinson

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E J Wadsworth

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P2860

A simple salting out procedure for extracting DNA from human nucleated cells

The 1993-94 Généthon human genetic linkage map

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus.

Fetal and infant growth and impaired glucose tolerance at age 64.

Permanent diabetes without serological evidence of autoimmunity after transient neonatal diabetes.

Insulin dependent diabetes in children under 5: incidence and ascertainment validation for 1992.

Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome.

The histopathology of the pancreas in type 1 (insulin-dependent) diabetes mellitus: a 25-year review of deaths in patients under 20 years of age in the United Kingdom.

Transient diabetes of the newborn.

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