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Wienker

Showing results (151-160 of 282) with videos related to

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Interdisciplinary Cardiovascular and Thoracic Surgery|October 1, 2024
Bilateral lung volume reduction surgery outperforms the unilateral approach in functional improvementÖzlem Okumus, Gernot Seebacher, Daniel Valdivia, et al.
Neuropediatrics|October 19, 2019
Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family-The Role of Next Generation Sequencing in Neuromuscular DisordersMaja von der Hagen, Lena-Luise Becker, Thomas F Wienker, et al.
American Journal of Human Genetics|September 23, 2000
Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15G Stöber, K Saar, F Rüschendorf, et al.
European Journal of Medical Genetics|June 8, 2020
An intronic splice site alteration in combination with a large deletion affecting VPS13B (COH1) causes Cohen syndromeFelix Boschann, Björn Fischer-Zirnsak, Thomas F Wienker, et al.
Molecular Psychiatry|February 13, 2002
Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locusJ Meyer, G Ortega, K Schraut, et al.
Plos One|August 27, 2015
The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri FamiliesBehzad Davarniya, Hao Hu, Kimia Kahrizi, et al.
Annals of Internal Medicine|August 8, 1998
Families with autosomal dominant brachydactyly type E, short stature, and severe hypertensionH R Toka, S Bähring, D Chitayat, et al.
Kidney International|February 7, 1998
A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactylyH Schuster, O Toka, H R Toka, et al.
Chest|September 11, 2009
VEGF gene haplotypes are associated with sarcoidosisStefan Pabst, Anna Karpushova, Amalia Diaz-Lacava, et al.
Journal of Neuroimmunology|March 17, 2004
Identification and functional characterization of a highly polymorphic region in the human TRAIL promoter in multiple sclerosisAlexandra Weber, Klaus-Peter Wandinger, Wolf Mueller, et al.
Pageof 29

Showing results (151-160 of 282) with videos related to

Sort By:
Pageof 29
Interdisciplinary Cardiovascular and Thoracic Surgery|October 1, 2024
Bilateral lung volume reduction surgery outperforms the unilateral approach in functional improvementÖzlem Okumus, Gernot Seebacher, Daniel Valdivia, et al.
Neuropediatrics|October 19, 2019
Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family-The Role of Next Generation Sequencing in Neuromuscular DisordersMaja von der Hagen, Lena-Luise Becker, Thomas F Wienker, et al.
American Journal of Human Genetics|September 23, 2000
Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15G Stöber, K Saar, F Rüschendorf, et al.
European Journal of Medical Genetics|June 8, 2020
An intronic splice site alteration in combination with a large deletion affecting VPS13B (COH1) causes Cohen syndromeFelix Boschann, Björn Fischer-Zirnsak, Thomas F Wienker, et al.
Molecular Psychiatry|February 13, 2002
Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locusJ Meyer, G Ortega, K Schraut, et al.
Plos One|August 27, 2015
The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri FamiliesBehzad Davarniya, Hao Hu, Kimia Kahrizi, et al.
Annals of Internal Medicine|August 8, 1998
Families with autosomal dominant brachydactyly type E, short stature, and severe hypertensionH R Toka, S Bähring, D Chitayat, et al.
Kidney International|February 7, 1998
A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactylyH Schuster, O Toka, H R Toka, et al.
Chest|September 11, 2009
VEGF gene haplotypes are associated with sarcoidosisStefan Pabst, Anna Karpushova, Amalia Diaz-Lacava, et al.
Journal of Neuroimmunology|March 17, 2004
Identification and functional characterization of a highly polymorphic region in the human TRAIL promoter in multiple sclerosisAlexandra Weber, Klaus-Peter Wandinger, Wolf Mueller, et al.
Pageof 29