Similar articles for PMID: 10071056

Year	Number of Results
1993	2
1994	1
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1997	5
1998	7
1999	17
2000	8
2001	9
2002	8
2003	10
2004	19
2005	8
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2010	10
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2013	4
2014	5
2015	6
2016	4
2017	6
2018	8
2019	11
2020	9
2021	12
2022	7
2023	3
2024	0

1

The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype.

De Jonghe P, Timmerman V, Ceuterick C, Nelis E, De Vriendt E, Löfgren A, Vercruyssen A, Verellen C, Van Maldergem L, Martin JJ, Van Broeckhoven C. De Jonghe P, et al. Brain. 1999 Feb;122 ( Pt 2):281-90. doi: 10.1093/brain/122.2.281. Brain. 1999. PMID: 10071056

2

Genetic epidemiology of Charcot-Marie-Tooth disease.

Braathen GJ. Braathen GJ. Acta Neurol Scand Suppl. 2012;(193):iv-22. doi: 10.1111/ane.12013. Acta Neurol Scand Suppl. 2012. PMID: 23106488

3

Charcot-Marie-Tooth neuropathy type 2 and P0 point mutations: two novel amino acid substitutions (Asp61Gly; Tyr119Cys) and a possible "hotspot" on Thr124Met.

Senderek J, Hermanns B, Lehmann U, Bergmann C, Marx G, Kabus C, Timmerman V, Stoltenburg-Didinger G, Schröder JM. Senderek J, et al. Brain Pathol. 2000 Apr;10(2):235-48. doi: 10.1111/j.1750-3639.2000.tb00257.x. Brain Pathol. 2000. PMID: 10764043 Free PMC article.

4

Charcot-Marie-Tooth families in Japan with MPZ Thr124Met mutation.

Kurihara S, Adachi Y, Imai C, Araki H, Hattori N, Numakura C, Lin Y, Hayasaka K, Sobue G, Nakashima K. Kurihara S, et al. J Neurol Neurosurg Psychiatry. 2004 Oct;75(10):1492-4. doi: 10.1136/jnnp.2003.020107. J Neurol Neurosurg Psychiatry. 2004. PMID: 15377707 Free PMC article.

5

An axonal form of Charcot-Marie-Tooth disease showing distinctive features in association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val).

Misu K, Yoshihara T, Shikama Y, Awaki E, Yamamoto M, Hattori N, Hirayama M, Takegami T, Nakashima K, Sobue G. Misu K, et al. J Neurol Neurosurg Psychiatry. 2000 Dec;69(6):806-11. doi: 10.1136/jnnp.69.6.806. J Neurol Neurosurg Psychiatry. 2000. PMID: 11080237 Free PMC article.

6

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.

Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, Ohnishi A, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakashima K, Kira J, Kaji R, Oka N, Sobue G; Study Group for Hereditary Neuropathy in Japan. Hattori N, et al. Brain. 2003 Jan;126(Pt 1):134-51. doi: 10.1093/brain/awg012. Brain. 2003. PMID: 12477701 Review.

7

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. 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.

8

[Two families of Charcot-Marie-Tooth disease with Adie's pupil, axonal neuropahy and the Thr124Met mutation in the peripheral myelin protein zero gene].

Misu K, Yoshihara T, Yamamoto M, Hattori N, Nagamatu M, Mukai E, Takegami T, Sobue G. Misu K, et al. Rinsho Shinkeigaku. 2000 Feb;40(2):149-54. Rinsho Shinkeigaku. 2000. PMID: 10835936 Japanese.

9

Charcot-Marie-Tooth disease: a novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family.

Leal A, Berghoff C, Berghoff M, Del Valle G, Contreras C, Montoya O, Hernández E, Barrantes R, Schlötzer-Schrehardt U, Neundörfer B, Reis A, Rautenstrauss B, Heuss D. Leal A, et al. Neurogenetics. 2003 Aug;4(4):191-7. doi: 10.1007/s10048-003-0153-0. Epub 2003 Jul 5. Neurogenetics. 2003. PMID: 12845552 Free article.

10

Autonomic and respiratory dysfunction in Charcot-Marie-Tooth disease due to Thr124Met mutation in the myelin protein zero gene.

Stojkovic T, de Seze J, Dubourg O, Arne-Bes MC, Tardieu S, Hache JC, Vermersch P. Stojkovic T, et al. Clin Neurophysiol. 2003 Sep;114(9):1609-14. doi: 10.1016/s1388-2457(03)00159-7. Clin Neurophysiol. 2003. PMID: 12948789

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