Search research articles
Contact Us
Filters
Showing results (801-810 of 949) with videos related to
Page
of 95
Sort By:
Neurogenetics
|
May 18, 1999
Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosis
C Fuchs, T Liehr, S Ozbey, et al.
Neurogenetics
|
May 18, 1999
Mapping, genomic structure, and polymorphisms of the human GABABR1 receptor gene: evaluation of its involvement in idiopathic generalized epilepsy
H C Peters, G Kämmer, A Volz, et al.
Neurogenetics
|
December 22, 2007
RNA interference of LRRK2-microarray expression analysis of a Parkinson's disease key player
K Häbig, M Walter, S Poths, et al.
Neurogenetics
|
February 12, 2014
The documentation of consent and disclosure of neurogenetic testing outside clinical genetics
C Lo, J Martindale, M Hadjivassiliou, et al.
Neurogenetics
|
March 24, 2025
Repeated clear benefits of immunotherapy in a patient with Charcot-Marie-Tooth disease carrying a rare point mutation in PMP22
Honami Kawai, Yoichiro Nishida, Takashi Kanda, et al.
Neurogenetics
|
March 5, 2025
Investigating the gut microbiome in schizophrenia cases versus controls: South Africa's version
Carlien Rust, Laila Asmal, Michaela O'Hare, et al.
Neurogenetics
|
November 28, 2024
Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69
Zahra Sadr, Aida Ghasemi, Mohammad Rohani, et al.
Neurogenetics
|
November 25, 2024
Understanding pathophysiology in fragile X syndrome: a comprehensive review
Juan Carlos Castillo Juárez, Alejandro Aguilar Gómez, Adrian Esteban Salatino Díaz, et al.
Neurogenetics
|
November 27, 2024
Giant axonal neuropathy: a rare inherited neuropathy with a novel mutation
Bita Poorshiri, Neda Jabbarpour, Mohammad Barzegar, et al.
Neurogenetics
|
February 15, 2025
Early-onset Parkinson's disease in a patient with a rare homozygous pathogenic GBA1 variant and no Gaucher disease symptoms
Juliana Cordovil Cotrin, Rafael Mina Piergiorge, Andressa Pereira Gonçalves, et al.
Page
of 95
Search research articles
Search
Showing results (801-810 of 949) with videos related to
Sort By:
Page
of 95
Neurogenetics
|
May 18, 1999
Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosis
C Fuchs, T Liehr, S Ozbey, et al.
Neurogenetics
|
May 18, 1999
Mapping, genomic structure, and polymorphisms of the human GABABR1 receptor gene: evaluation of its involvement in idiopathic generalized epilepsy
H C Peters, G Kämmer, A Volz, et al.
Neurogenetics
|
December 22, 2007
RNA interference of LRRK2-microarray expression analysis of a Parkinson's disease key player
K Häbig, M Walter, S Poths, et al.
Neurogenetics
|
February 12, 2014
The documentation of consent and disclosure of neurogenetic testing outside clinical genetics
C Lo, J Martindale, M Hadjivassiliou, et al.
Neurogenetics
|
March 24, 2025
Repeated clear benefits of immunotherapy in a patient with Charcot-Marie-Tooth disease carrying a rare point mutation in PMP22
Honami Kawai, Yoichiro Nishida, Takashi Kanda, et al.
Neurogenetics
|
March 5, 2025
Investigating the gut microbiome in schizophrenia cases versus controls: South Africa's version
Carlien Rust, Laila Asmal, Michaela O'Hare, et al.
Neurogenetics
|
November 28, 2024
Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69
Zahra Sadr, Aida Ghasemi, Mohammad Rohani, et al.
Neurogenetics
|
November 25, 2024
Understanding pathophysiology in fragile X syndrome: a comprehensive review
Juan Carlos Castillo Juárez, Alejandro Aguilar Gómez, Adrian Esteban Salatino Díaz, et al.
Neurogenetics
|
November 27, 2024
Giant axonal neuropathy: a rare inherited neuropathy with a novel mutation
Bita Poorshiri, Neda Jabbarpour, Mohammad Barzegar, et al.
Neurogenetics
|
February 15, 2025
Early-onset Parkinson's disease in a patient with a rare homozygous pathogenic GBA1 variant and no Gaucher disease symptoms
Juliana Cordovil Cotrin, Rafael Mina Piergiorge, Andressa Pereira Gonçalves, et al.
Page
of 95