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Wolfram s syndrome DIDMOAD
LE WE PMID CA
Wolfram s syndrome DIDMOAD2931Wolfram Syndrom DIDMOAD

ABCC8 SUR1

Anemia (megaloblastic thiamine responsive)

Bererdinelli Seip congenital lipodystrophy

BSCL1 AGPAT2

BSCL2 Seipin

Diabetes mellitus (Beta cell decay)

Diabetes mellitus (Hereditary MODY)

Diabetes mellitus (hereditary)

Diabetes mellitus (neonatal)

Donohue s syndrome Leprechaunism

EIF2AK3 PERK

ERS UFR (Induced Mediators)

FRDA1 Frataxin

Friedreich ataxia

Glucokinase

GLUD1

Insulin resistance type a

KCNJ11 Kir6 2

Lipodystrophy

OMIM_601487

OMIM_x600937

Persistent hyperinsulinemic hypoglycemia of infancy

Persistent neonatal hypoglycemia

Rabson Mendenhall s syndrome

Receptor (Insulin)

Receptor (PPAR gamma)

SLC19A2 THTR1

TNDM29locus

Werner s syndrome

Wfs1 Wolframin

Wfs2

Wolcott Rallison syndrome

Wolfram s syndrome DIDMOAD

WRN

1997  
1
2007  
2
[Two cases of Wolfram syndrome].
[17646750] J Fr Ophtalmol 30(6): 607-9 (2007)
2005  
3
Endoplasmic reticulum stress induces Wfs1 gene expression in pancreatic beta-cells via transcriptional activation.
[15994758] Eur J Endocrinol 153(1): 167-76 (2005)
2005  
4
Monogenic syndromes of abnormal glucose homeostasis: clinical review and relevance to the understanding of the pathology of insulin resistance and beta cell failure.
[15772126] J Med Genet 42(12): 893-902 (2005)

Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth

All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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