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I Samman

Showing results (1-10 of 8) with videos related to

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Lancet (London, England)|March 21, 1998
Rational therapy of Guillain-Barré syndromeI Samman, J C Wöhrle, M Hennerici
Deutsche Medizinische Wochenschrift (1946)|June 10, 1998
[Neurologic cause for a respiratory insufficiency]S Ries, J C Wöhrle, I Samman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 16, 1999
Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2I Samman, W J Schulz-Schaeffer, J C Wöhrle, et al.
Journal of Human Genetics|November 6, 2015
Homozygous sequence variants in the FKBP10 gene underlie osteogenesis imperfecta in consanguineous familiesMuhammad Umair, Annum Hassan, Abid Jan, et al.
Annals of Saudi Medicine|December 7, 2016
A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephalyJamil A Hashmi, Khalid M Al-Harbi, Khushnooda Ramzan, et al.
Human Genetics|August 14, 2016
CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephalySulman Basit, Khalid M Al-Harbi, Sabri A M Alhijji, et al.
Neuroscience|November 7, 2016
High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex familiesLaila Y AlAyadhi, Jamil A Hashmi, Muhammad Iqbal, et al.
BMC Ophthalmology|October 8, 2016
Sequence analysis of four vitamin D family genes (VDR, CYP24A1, CYP27B1 and CYP2R1) in Vogt-Koyanagi-Harada (VKH) patients: identification of a potentially pathogenic variant in CYP2R1Ma'an Abdullah Al-Barry, Alia M Albalawi, Mohammed Abu Sayf, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Lancet (London, England)|March 21, 1998
Rational therapy of Guillain-Barré syndromeI Samman, J C Wöhrle, M Hennerici
Deutsche Medizinische Wochenschrift (1946)|June 10, 1998
[Neurologic cause for a respiratory insufficiency]S Ries, J C Wöhrle, I Samman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 16, 1999
Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2I Samman, W J Schulz-Schaeffer, J C Wöhrle, et al.
Journal of Human Genetics|November 6, 2015
Homozygous sequence variants in the FKBP10 gene underlie osteogenesis imperfecta in consanguineous familiesMuhammad Umair, Annum Hassan, Abid Jan, et al.
Annals of Saudi Medicine|December 7, 2016
A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephalyJamil A Hashmi, Khalid M Al-Harbi, Khushnooda Ramzan, et al.
Human Genetics|August 14, 2016
CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephalySulman Basit, Khalid M Al-Harbi, Sabri A M Alhijji, et al.
Neuroscience|November 7, 2016
High-resolution SNP genotyping platform identified recurrent and novel CNVs in autism multiplex familiesLaila Y AlAyadhi, Jamil A Hashmi, Muhammad Iqbal, et al.
BMC Ophthalmology|October 8, 2016
Sequence analysis of four vitamin D family genes (VDR, CYP24A1, CYP27B1 and CYP2R1) in Vogt-Koyanagi-Harada (VKH) patients: identification of a potentially pathogenic variant in CYP2R1Ma'an Abdullah Al-Barry, Alia M Albalawi, Mohammed Abu Sayf, et al.
Pageof 1