Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

8 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.
De Sandre-Giovannoli A, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, Hammadouche T, Vandenberghe A, Stewart CL, Grid D, Lévy N. De Sandre-Giovannoli A, et al. Among authors: hammadouche t. Am J Hum Genet. 2002 Mar;70(3):726-36. doi: 10.1086/339274. Epub 2002 Jan 17. Am J Hum Genet. 2002. PMID: 11799477 Free PMC article.
The autosomal recessive form of CMT disease linked to 5q31-q33.
Guilbot A, Kessali M, Ravisé N, Hammadouche T, Bouhouche A, Maisonobe T, Grid D, Brice A, Leguern E. Guilbot A, et al. Among authors: hammadouche t. Ann N Y Acad Sci. 1999 Sep 14;883:56-9. Ann N Y Acad Sci. 1999. PMID: 10586230 No abstract available.
The autosomal recessive form of CMT disease linked to 5q31-q33.
Guilbot A, Kessali M, Ravisé N, Hammadouche T, Bouhouche A, Maisonobe T, Grid D, Brice A, LeGuern E. Guilbot A, et al. Among authors: hammadouche t. Ann N Y Acad Sci. 1999 Sep 14;883:453-6. Ann N Y Acad Sci. 1999. PMID: 10586271 No abstract available.
The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33.
Guilbot A, Kessali M, Ravisé N, Hammadouche T, Bouhouche A, Maisonobe T, Grid D, Brice A, LeGUERN E. Guilbot A, et al. Among authors: hammadouche t. Ann N Y Acad Sci. 1999 Oct;883(1):453-456. doi: 10.1111/j.1749-6632.1999.tb08608.x. Ann N Y Acad Sci. 1999. PMID: 29086961 No abstract available.
The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33.
Guilbot A, Kessali M, Ravisé N, Hammadouche T, Bouhouche A, Maisonobe T, Grid D, Brice A, Leguern E. Guilbot A, et al. Among authors: hammadouche t. Ann N Y Acad Sci. 1999 Oct;883(1):56-59. doi: 10.1111/j.1749-6632.1999.tb08567.x. Ann N Y Acad Sci. 1999. PMID: 29086979 No abstract available.
Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma.
Azzedine H, Bolino A, Taïeb T, Birouk N, Di Duca M, Bouhouche A, Benamou S, Mrabet A, Hammadouche T, Chkili T, Gouider R, Ravazzolo R, Brice A, Laporte J, LeGuern E. Azzedine H, et al. Among authors: hammadouche t. Am J Hum Genet. 2003 May;72(5):1141-53. doi: 10.1086/375034. Epub 2003 Apr 8. Am J Hum Genet. 2003. PMID: 12687498 Free PMC article.