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Scholar Results 1 - 10 of about 124 citing Guillausseau: Maternally inherited diabetes and deafness: a multicenter study. (0.15 sec) 

[PDF] Special Article-Nonalcoholic Steatohepatitis: Summary of an AASLD Single Topic …


BA Neuschwander-Tetri, SH Caldwell - Hepatology, 2003 - ualberta.ca
Fatty liver disease that develops in the absence of alcohol abuse is recognized
increasingly as a major health burden. This report summarizes the presentations
and discussions at a Single Topic Conference held September 20-22, 2002, ...
Cited by 828 - Related articles - View as HTML - BL Direct - All 9 versions

Mitochondrial deafness


N Fischel-Ghodsian - Ear and hearing, 2003 - journals.lww.com
The last decade has led to the identification of several mitochondrial DNA
mutations associated with hearing loss. Since the only known function of the
human mitochondrial chromosome is to partic- ipate in the production of ...
Cited by 60 - Related articles - BL Direct - All 4 versions

Mitochondria in nonalcoholic fatty liver disease


SH Caldwell, CY Chang, RK Nakamoto, L … - Clinics in liver disease, 2004 - Elsevier
Nonalcoholic fatty liver (NAFL) is associated with fundamental issues of fat
metabolism and insulin resistance. These abnormalities have been linked to
impairment of ATP homeostasis, and a growing body of literature has ...
Cited by 51 - Related articles - BL Direct - All 3 versions

Molecular etiologies of MODY and other early-onset forms of diabetes


DQ Shih, M Stoffel - Current Diabetes Reports, 2002 - Springer
Introduction Despite the minute size of the pancreatic islets, the endo- crine
pancreas is a critical organ for maintaining glucose homeostasis and it plays a
key role in the etiology of type 1 and type 2 diabetes mellitus. Type 1 ...
Cited by 46 - Related articles - All 3 versions

The contribution of mitochondria to common disorders


GM Enns - Molecular genetics and metabolism, 2003 - Elsevier
Mitochondrial dysfunction secondary to mitochondrial and nuclear DNA mutations
has been associated with energy deficiency in multiple organ systems and a
variety of severe, often fatal, clinical syndromes. Although the production ...
Cited by 42 - Related articles - All 4 versions

Molecular mechanisms of mitochondrial diabetes (MIDD)


JA Maassen, GMC Janssen, LM 't Hart - Annals of Medicine, 2005 - informahealthcare.com
Abstract Mitochondria provide cells with most of the energy in the form of
adenosine triphosphate (ATP). Mitochondria are complex organelles encoded both
by nuclear and mtDNA. Only a few mitochondrial components are encoded by ...
Cited by 38 - Related articles - All 6 versions

Mitochondrial diabetes: pathophysiology, clinical presentation, and genetic analysis


JA Maassen - American journal of medical genetics, 2002 - interscience.wiley.com
It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ...
Cited by 36 - Related articles - BL Direct - All 3 versions

Clinical implications of a molecular genetic classification of monogenic β-cell diabetes


R Murphy, S Ellard, AT Hattersley - Nature Clinical Practice Endocrinology & Metabolism, 2008 - nature.com
Sian Ellard is Professor of Human Molecular Genetics, Peninsula Medical School,
Exeter, UK. Following research training at the University of Swansea (UK), she
set up the Molecular Genetics Laboratory in Exeter with Professor Andrew ...
Cited by 31 - Related articles - BL Direct - All 6 versions

The spectrum of systemic involvement in adults presenting with renal lesion and …

- asnjournals.org
B Guery, G Choukroun, LH Noel, P Clavel, A … - Journal of the American Society of Nephrology, 2003 - Am Soc Nephrol
*Service de Néphrologie and INSERM U507, Hôpital Necker, Paris; Service de
Néphrologie, Hôpital Sud, Amiens; Service de Néphrologie, Hôpital de
Brabois, Vandoeuvre-lès-Nancy; Département de Génétique Médicale and ...
Cited by 31 - Related articles - BL Direct - All 7 versions

Clinical features of diabetes mellitus with the mitochondrial DNA 3243 (A–G) mutation in …


S Suzuki, Y Oka, T Kadowaki, A Kanatsuka, T … - Diabetes research and clinical practice, 2003 - Elsevier
Diabetes mellitus with the mitochondrial DNA 3243(A–G) mutation is reported to
represent 0.5–2.8% of the general diabetic population. Since the
characterization of diabetes with the mutation is still incomplete, we ...
Cited by 27 - Related articles - All 6 versions


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