de Visser M - Search Results

1

Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease.

Meggouh F, de Visser M, Arts WF, De Coo RI, van Schaik IN, Baas F. Meggouh F, et al. Among authors: de visser m, de coo ri. Ann Neurol. 2005 Apr;57(4):589-91. doi: 10.1002/ana.20434. Ann Neurol. 2005. PMID: 15786462

2

Comparison of CMT1A and CMT2: similarities and differences.

Bienfait HM, Verhamme C, van Schaik IN, Koelman JH, de Visser BW, de Haan RJ, Baas F, van Engelen BG, de Visser M. Bienfait HM, et al. Among authors: de visser bw, de visser m, de haan rj. J Neurol. 2006 Dec;253(12):1572-80. doi: 10.1007/s00415-006-0260-6. Epub 2006 Aug 28. J Neurol. 2006. PMID: 16941080

3

Clinical disease severity and axonal dysfunction in hereditary motor and sensory neuropathy Ia.

Verhamme C, van Schaik IN, Koelman JH, de Haan RJ, Vermeulen M, de Visser M. Verhamme C, et al. Among authors: de visser m, de haan rj. J Neurol. 2004 Dec;251(12):1491-7. doi: 10.1007/s00415-004-0578-x. J Neurol. 2004. PMID: 15645349

4

Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathies.

Meijerink PH, Hoogendijk JE, Gabreëls-Festen AA, Zorn I, Veldman H, Baas F, de Visser M, Bolhuis PA. Meijerink PH, et al. Among authors: de visser m. Ann Neurol. 1996 Oct;40(4):672-5. doi: 10.1002/ana.410400418. Ann Neurol. 1996. PMID: 8871588 Free article.

5

Late onset axonal Charcot-Marie-Tooth phenotype caused by a novel myelin protein zero mutation.

Bienfait HM, Faber CG, Baas F, Gabreëls-Festen AA, Koelman JH, Hoogendijk JE, Verschuuren JJ, Wokke JH, de Visser M. Bienfait HM, et al. Among authors: de visser m. J Neurol Neurosurg Psychiatry. 2006 Apr;77(4):534-7. doi: 10.1136/jnnp.2005.073437. J Neurol Neurosurg Psychiatry. 2006. PMID: 16543539 Free PMC article.

6

Charcot-Marie-Tooth disease due to a de novo mutation of the RAB7 gene.

Meggouh F, Bienfait HM, Weterman MA, de Visser M, Baas F. Meggouh F, et al. Among authors: de visser m. Neurology. 2006 Oct 24;67(8):1476-8. doi: 10.1212/01.wnl.0000240068.21499.f5. Neurology. 2006. PMID: 17060578

7

Phenotype of Charcot-Marie-Tooth disease Type 2.

Bienfait HM, Baas F, Koelman JH, de Haan RJ, van Engelen BG, Gabreëls-Festen AA, Ongerboer de Visser BW, Meggouh F, Weterman MA, De Jonghe P, Timmerman V, de Visser M. Bienfait HM, et al. Among authors: de jonghe p, de visser m, de haan rj. Neurology. 2007 May 15;68(20):1658-67. doi: 10.1212/01.wnl.0000263479.97552.94. Neurology. 2007. PMID: 17502546

8

Motor axon loss is associated with hand dysfunction in Charcot-Marie-Tooth disease 1a.

Videler AJ, van Dijk JP, Beelen A, de Visser M, Nollet F, van Schaik IN. Videler AJ, et al. Among authors: de visser m. Neurology. 2008 Oct 14;71(16):1254-60. doi: 10.1212/01.wnl.0000327643.05073.eb. Neurology. 2008. PMID: 18852440

9

Manual dexterity in hereditary motor and sensory neuropathy type 1a: severity of limitations and feasibility and reliability of two assessment instruments.

Videler AJ, Beelen A, van Schaik IN, de Visser M, Nollet F. Videler AJ, et al. Among authors: de visser m. J Rehabil Med. 2008 Feb;40(2):132-6. doi: 10.2340/16501977-0143. J Rehabil Med. 2008. PMID: 18509578 Free article.

10

Limited upper limb functioning has impact on restrictions in participation and autonomy of patients with hereditary motor and sensory neuropathy 1a.

Videler AJ, Beelen A, van Schaik IN, de Visser M, Nollet F. Videler AJ, et al. Among authors: de visser m. J Rehabil Med. 2009 Sep;41(9):746-50. doi: 10.2340/16501977-0419. J Rehabil Med. 2009. PMID: 19774309 Free article.

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