Hamadouche T[au] - Search Results

Year	Number of Results
1998	1
2000	2
2003	2
2004	1
2005	1
2006	2
2007	2
2008	1
2009	1
2010	2
2011	2
2012	3
2013	1
2014	1
2015	1
2023	1
2024	0

1

Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update.

Tazir M, Hamadouche T, Nouioua S, Mathis S, Vallat JM. Tazir M, et al. Among authors: hamadouche t. J Neurol Sci. 2014 Dec 15;347(1-2):14-22. doi: 10.1016/j.jns.2014.10.013. Epub 2014 Oct 16. J Neurol Sci. 2014. PMID: 25454638 Review.

2

Weight Status Prediction Using a Neuron Network Based on Individual and Behavioral Data.

Rousset S, Angelo A, Hamadouche T, Lacomme P. Rousset S, et al. Among authors: hamadouche t. Healthcare (Basel). 2023 Apr 12;11(8):1101. doi: 10.3390/healthcare11081101. Healthcare (Basel). 2023. PMID: 37107935 Free PMC article.

3

Phenotypic variability in giant axonal neuropathy.

Tazir M, Nouioua S, Magy L, Huehne K, Assami S, Urtizberea A, Grid D, Hamadouche T, Rautenstrauss B, Vallat JM. Tazir M, et al. Among authors: hamadouche t. Neuromuscul Disord. 2009 Apr;19(4):270-4. doi: 10.1016/j.nmd.2009.01.011. Epub 2009 Feb 23. Neuromuscul Disord. 2009. PMID: 19231187

4

Pantothenate kinase-associated neurodegeneration: clinical description of 10 patients and identification of new mutations.

Assami S, Azzedine H, Nouioua S, Mundwiller E, Mahoui S, Makri S, Djemai M, Grid D, Brice A, Hamadouche T, Stevanin G, Tazir M. Assami S, et al. Among authors: hamadouche t. Mov Disord. 2011 Aug 1;26(9):1777-9. doi: 10.1002/mds.23648. Epub 2011 Mar 25. Mov Disord. 2011. PMID: 21442655 No abstract available.

5

Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes.

Nouioua S, Hamadouche T, Funalot B, Bernard R, Bellatache N, Bouderba R, Grid D, Assami S, Benhassine T, Levy N, Vallat JM, Tazir M. Nouioua S, et al. Among authors: hamadouche t. Neuromuscul Disord. 2011 Aug;21(8):543-50. doi: 10.1016/j.nmd.2011.04.013. Epub 2011 Jul 7. Neuromuscul Disord. 2011. PMID: 21741241

6

Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.

Hamza W, Ali Pacha L, Hamadouche T, Muller J, Drouot N, Ferrat F, Makri S, Chaouch M, Tazir M, Koenig M, Benhassine T. Hamza W, et al. Among authors: hamadouche t. BMC Med Genet. 2015 Jun 12;16:36. doi: 10.1186/s12881-015-0180-3. BMC Med Genet. 2015. PMID: 26068213 Free PMC article.

7

Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.

Lesage S, Patin E, Condroyer C, Leutenegger AL, Lohmann E, Giladi N, Bar-Shira A, Belarbi S, Hecham N, Pollak P, Ouvrard-Hernandez AM, Bardien S, Carr J, Benhassine T, Tomiyama H, Pirkevi C, Hamadouche T, Cazeneuve C, Basak AN, Hattori N, Dürr A, Tazir M, Orr-Urtreger A, Quintana-Murci L, Brice A; French Parkinson's Disease Genetics Study Group. Lesage S, et al. Among authors: hamadouche t. Hum Mol Genet. 2010 May 15;19(10):1998-2004. doi: 10.1093/hmg/ddq081. Epub 2010 Mar 2. Hum Mol Genet. 2010. PMID: 20197411

8

Behavioral and molecular exploration of the AR-CMT2A mouse model Lmna (R298C/R298C).

Poitelon Y, Kozlov S, Devaux J, Vallat JM, Jamon M, Roubertoux P, Rabarimeriarijaona S, Baudot C, Hamadouche T, Stewart CL, Levy N, Delague V. Poitelon Y, et al. Among authors: hamadouche t. Neuromolecular Med. 2012 Mar;14(1):40-52. doi: 10.1007/s12017-012-8168-z. Epub 2012 Feb 14. Neuromolecular Med. 2012. PMID: 22331516

9

Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations.

Azzedine H, Ravisé N, Verny C, Gabrëels-Festen A, Lammens M, Grid D, Vallat JM, Durosier G, Senderek J, Nouioua S, Hamadouche T, Bouhouche A, Guilbot A, Stendel C, Ruberg M, Brice A, Birouk N, Dubourg O, Tazir M, LeGuern E. Azzedine H, et al. Among authors: hamadouche t. Neurology. 2006 Aug 22;67(4):602-6. doi: 10.1212/01.wnl.0000230225.19797.93. Neurology. 2006. PMID: 16924012

10

Two novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H).

Baudot C, Esteve C, Castro C, Poitelon Y, Mas C, Hamadouche T, El-Rajab M, Lévy N, Megarbané A, Delague V. Baudot C, et al. Among authors: hamadouche t. J Peripher Nerv Syst. 2012 Jun;17(2):141-6. doi: 10.1111/j.1529-8027.2012.00405.x. J Peripher Nerv Syst. 2012. PMID: 22734899

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