These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 38479034)

  • 1. Hereditary motor and sensory neuropathy Okinawa type mimicking proximal myopathy.
    Braga VL; Tamanini JVG; Gama SM; Fraiman PHA; Silva TYT; Santos-Neto D; Barsottini OGP; Pedroso JL
    Clin Neurol Neurosurg; 2024 Apr; 239():108213. PubMed ID: 38479034
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary motor and sensory neuropathy (proximal dominant form, HMSN-P) among Brazilians of Japanese ancestry.
    Maeda K; Sugiura M; Kato H; Sanada M; Kawai H; Yasuda H
    Clin Neurol Neurosurg; 2007 Nov; 109(9):830-2. PubMed ID: 17764830
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Two cases of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P)].
    Mori C; Saito T; Saito T; Fujimura H; Sakoda S
    Rinsho Shinkeigaku; 2015; 55(6):401-5. PubMed ID: 26103812
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Survey of patients with advanced-stage Okinawa-type neurogenic muscular atrophy (hereditary motor and sensory neuropathy with proximal dominant involvement: HMSN-P)].
    Taniguchi M; Yorishima Y; Shoji H; Ide M; Kumura Y; Kunisaki K
    Rinsho Shinkeigaku; 2022 Feb; 62(2):152-156. PubMed ID: 35095044
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Proximal Dominant Hereditary Motor and Sensory Neuropathy with
    Ansari AF; Jagiasi K; Ojha P; Ansari R; Nagendra S; Kharat S
    Neurol India; 2022; 70(3):1220-1222. PubMed ID: 35864671
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal dominant HMSN with proximal involvement: new Brazilian cases.
    Patroclo CB; Lino AM; Marchiori PE; Brotto MW; Hirata MT
    Arq Neuropsiquiatr; 2009 Sep; 67(3B):892-6. PubMed ID: 19838524
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) is caused by a mutation in TFG].
    Ishiura H; Tsuji S
    Rinsho Shinkeigaku; 2013; 23(11):1203-5. PubMed ID: 24291930
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The TRK-fused gene is mutated in hereditary motor and sensory neuropathy with proximal dominant involvement.
    Ishiura H; Sako W; Yoshida M; Kawarai T; Tanabe O; Goto J; Takahashi Y; Date H; Mitsui J; Ahsan B; Ichikawa Y; Iwata A; Yoshino H; Izumi Y; Fujita K; Maeda K; Goto S; Koizumi H; Morigaki R; Ikemura M; Yamauchi N; Murayama S; Nicholson GA; Ito H; Sobue G; Nakagawa M; Kaji R; Tsuji S
    Am J Hum Genet; 2012 Aug; 91(2):320-9. PubMed ID: 22883144
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sural nerve pathology in TFG-associated motor neuron disease with sensory neuropathy.
    Li J; Meng L; Wu R; Xie Z; Gang Q; Zhang W; Wang Z; Yuan Y
    Neuropathology; 2019 Jun; 39(3):194-199. PubMed ID: 30957313
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Wide spectrum of hereditary motor sensory neuropathy (HMSN)].
    Nakagawa M
    Rinsho Shinkeigaku; 2009 Nov; 49(11):950-2. PubMed ID: 20030257
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Proximal dominant hereditary motor and sensory neuropathy with proximal dominance association with mutation in the TRK-fused gene.
    Lee SS; Lee HJ; Park JM; Hong YB; Park KD; Yoo JH; Koo H; Jung SC; Park HS; Lee JH; Lee MG; Hyun YS; Nakhro K; Chung KW; Choi BO
    JAMA Neurol; 2013 May; 70(5):607-15. PubMed ID: 23553329
    [TBL] [Abstract][Full Text] [Related]  

  • 12. HMSN-P caused by p.Pro285Leu mutation in TFG is not confined to patients with Far East ancestry.
    Alavi A; Shamshiri H; Nafissi S; Khani M; Klotzle B; Fan JB; Steemers F; Elahi E
    Neurobiol Aging; 2015 Mar; 36(3):1606.e1-7. PubMed ID: 25725944
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneity.
    Maeda K; Kaji R; Yasuno K; Jambaldorj J; Nodera H; Takashima H; Nakagawa M; Makino S; Tamiya G
    J Hum Genet; 2007; 52(11):907-914. PubMed ID: 17906970
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [History of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P)].
    Takashima H
    Rinsho Shinkeigaku; 2013; 23(11):1196-8. PubMed ID: 24291927
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary motor sensory neuropathy with proximal involvement (HMSN-P) associated with TFG p.Pro285Leu variant in an Italian family with a motor neuron disease-like clinical picture.
    Cabras S; Di Pede F; Canosa A; Grassano M; Mongini TE; Gadaleta G; Calvo A; Chiò A; Moglia C; Gallone S
    Muscle Nerve; 2024 Jun; 69(6):730-732. PubMed ID: 38533668
    [No Abstract]   [Full Text] [Related]  

  • 16. Muscle pathology of hereditary motor and sensory neuropathy with proximal dominant involvement with TFG mutation.
    Yamashita S; Kimura E; Zhang Z; Tawara N; Hara K; Yoshimura A; Takashima H; Ando Y
    Muscle Nerve; 2019 Dec; 60(6):739-744. PubMed ID: 31449671
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new type of hereditary motor and sensory neuropathy linked to chromosome 3.
    Takashima H; Nakagawa M; Nakahara K; Suehara M; Matsuzaki T; Higuchi I; Higa H; Arimura K; Iwamasa T; Izumo S; Osame M
    Ann Neurol; 1997 Jun; 41(6):771-80. PubMed ID: 9189038
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of novel TFG mutation in HMSN-P pedigree: Emphasis on variable clinical presentations.
    Khani M; Shamshiri H; Alavi A; Nafissi S; Elahi E
    J Neurol Sci; 2016 Oct; 369():318-323. PubMed ID: 27653917
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Continuum of phenotypes in hereditary motor and sensory neuropathy with proximal predominance and Charcot-Marie-Tooth patients with TFG mutation.
    Khani M; Taheri H; Shamshiri H; Houlden H; Efthymiou S; Alavi A; Nafissi S; Elahi E
    Am J Med Genet A; 2019 Aug; 179(8):1507-1515. PubMed ID: 31111683
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary motor and sensory neuropathy IIB: clinical and electrodiagnostic characteristics.
    Elliott JL; Kwon JM; Goodfellow PJ; Yee WC
    Neurology; 1997 Jan; 48(1):23-8. PubMed ID: 9008488
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.