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Ali-Reza Moslemi

Senior lecturer

Ali-Reza Moslemi
Senior lecturer
ali-reza.moslemi@pathology.gu.se
+46 31 786 2906

Postal Address: Box 440, 40530 Göteborg
Visiting Address: Medicinaregatan 9 a-b , 41390 Göteborg


Institute of Biomedicine (More Information)
Box 440
405 30 Göteborg
www.biomedicine.gu.se
biomedicine@gu.se
Visiting Address: Medicinaregatan 9 A-B , 413 90 Göteborg

Latest publications

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy
N. Chatron, F. Becker, H. Morsy, M. Schmidts, K. Hardies et al.
Brain, Journal article 2020
Journal article

Expression of the GBGT1 Gene and the Forssman Antigen in Red Blood Cells in a Palestinian Population
W. A. Abusibaa, M. A. Srour, Ali-Reza Moslemi, Lola Svensson, C. Jesus et al.
Transfusion Medicine and Hemotherapy, Journal article 2019
Journal article

Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study
M. Sedghi, Ali-Reza Moslemi, M. Olive, M. Etemadifar, B. Ansari et al.
Annals of Clinical and Translational Neurology, Journal article 2019
Journal article

Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia
A. Kariminejad, E. Szenker-Ravi, C. Lekszas, H. Tajsharghi, Ali-Reza Moslemi et al.
American Journal of Human Genetics, Journal article 2019
Journal article

Ataxia-telangiectasia-like disorder in a family deficient for MRE11A, caused by a MRE11 variant
M. Sedghi, M. Salari, Ali-Reza Moslemi, A. Kariminejad, M. Davis et al.
Neurology-Genetics, Journal article 2018
Journal article

Prevalence of antibodies to a new histo-blood system: the FORS system
C. Jesus, Camilla Hesse, C. Rocha, N. Osorio, A. Valado et al.
Blood Transfusion, Journal article 2018
Journal article

Lethal multiple pterygium syndrome, the extreme end of the RYR1 spectrum
A. Kariminejad, S. Ghaderi-Sohi, H. H. N. Nedai, V. Varasteh, Ali-Reza Moslemi et al.
Bmc Musculoskeletal Disorders, Journal article 2016
Journal article

Showing 1 - 10 of 48

2020

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy
N. Chatron, F. Becker, H. Morsy, M. Schmidts, K. Hardies et al.
Brain, Journal article 2020
Journal article

2019

Expression of the GBGT1 Gene and the Forssman Antigen in Red Blood Cells in a Palestinian Population
W. A. Abusibaa, M. A. Srour, Ali-Reza Moslemi, Lola Svensson, C. Jesus et al.
Transfusion Medicine and Hemotherapy, Journal article 2019
Journal article

Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study
M. Sedghi, Ali-Reza Moslemi, M. Olive, M. Etemadifar, B. Ansari et al.
Annals of Clinical and Translational Neurology, Journal article 2019
Journal article

Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia
A. Kariminejad, E. Szenker-Ravi, C. Lekszas, H. Tajsharghi, Ali-Reza Moslemi et al.
American Journal of Human Genetics, Journal article 2019
Journal article

2018

Ataxia-telangiectasia-like disorder in a family deficient for MRE11A, caused by a MRE11 variant
M. Sedghi, M. Salari, Ali-Reza Moslemi, A. Kariminejad, M. Davis et al.
Neurology-Genetics, Journal article 2018
Journal article

Prevalence of antibodies to a new histo-blood system: the FORS system
C. Jesus, Camilla Hesse, C. Rocha, N. Osorio, A. Valado et al.
Blood Transfusion, Journal article 2018
Journal article

2017

2016

Lethal multiple pterygium syndrome, the extreme end of the RYR1 spectrum
A. Kariminejad, S. Ghaderi-Sohi, H. H. N. Nedai, V. Varasteh, Ali-Reza Moslemi et al.
Bmc Musculoskeletal Disorders, Journal article 2016
Journal article

Showing 1 - 10 of 48

Page Manager: Evelyn Vilkman|Last update: 2/5/2020
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