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Human Molecular Genetics|November 18, 1998
Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane proteinT M Strom, K Hörtnagel, S Hofmann, et al.
Infection|October 6, 2007
"Recreational" drug abuse associated with failure to mount a proper antibody response after a generalised orthopoxvirus infectionH P Huemer, A Himmelreich, B Hönlinger, et al.
Regulatory Peptides|August 30, 2008
Chromogranin peptides in amyotrophic lateral sclerosisA Schrott-Fischer, M Bitsche, C Humpel, et al.
Diabetologia|May 1, 1993
On the appearance of islet associated autoimmunity in offspring of diabetic mothers: a prospective study from birthA G Ziegler, B Hillebrand, W Rabl, et al.
American Journal of Human Genetics|April 1, 1995
Mutations in the gene for X-linked adrenoleukodystrophy in patients with different clinical phenotypesA Braun, H Ambach, S Kammerer, et al.
Genomics|January 1, 1997
Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypesS Hofmann, R Bezold, M Jaksch, et al.
Wiener Klinische Wochenschrift|April 14, 2000
[SIDS prevention program in Tyrol]W Sperl, U Kiechl-Kohlendorfer, U Pupp, et al.
APMIS : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica|December 21, 2007
Atrial natriuretic peptide and CD34 overexpression in human idiopathic dilated cardiomyopathiesN Ardizzone, F Cappello, V Di Felice, et al.
Archives of Orthopaedic and Trauma Surgery|March 25, 2006
Migration of two different cementless hip arthroplasty stems in combination with two different heads: a biomechanical in vitro studyT Klestil, M M Morlock, K Schwieger, et al.
Nature|December 15, 1994
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadismF Muscatelli, T M Strom, A P Walker, et al.
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