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W Rabl

Showing results (81-90 of 94) with videos related to

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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.
Journal of Biophotonics|July 26, 2023
Raman spectroscopy for postmortem interval estimation of human skeletal remains: A scoping reviewC Woess, Christian W Huck, J Badzoka, et al.
Human Molecular Genetics|February 1, 1995
Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious pubertyS Kosugi, C Van Dop, M E Geffner, et al.
Science (New York, N.Y.)|April 21, 1995
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, N Wohllk, et al.
Pageof 10

Showing results (81-90 of 94) with videos related to

Sort By:
Pageof 10
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.
Journal of Biophotonics|July 26, 2023
Raman spectroscopy for postmortem interval estimation of human skeletal remains: A scoping reviewC Woess, Christian W Huck, J Badzoka, et al.
Human Molecular Genetics|February 1, 1995
Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious pubertyS Kosugi, C Van Dop, M E Geffner, et al.
Science (New York, N.Y.)|April 21, 1995
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, N Wohllk, et al.
Pageof 10