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 *

250 related articles for article (PubMed ID: 10653194)

  • 61. Phenotypic clustering in MPZ mutations.
    Shy ME; Jáni A; Krajewski K; Grandis M; Lewis RA; Li J; Shy RR; Balsamo J; Lilien J; Garbern JY; Kamholz J
    Brain; 2004 Feb; 127(Pt 2):371-84. PubMed ID: 14711881
    [TBL] [Abstract][Full Text] [Related]  

  • 62. A Japanese family with early-onset ataxia with motor and sensory neuropathy.
    Kobayashi S; Takuma H; Murayama S; Sakurai M; Kanazawa I
    J Neurol Sci; 2007 Mar; 254(1-2):44-8. PubMed ID: 17258771
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1.
    Pitt M; Houlden H; Jacobs J; Mok Q; Harding B; Reilly M; Surtees R
    Brain; 2003 Dec; 126(Pt 12):2682-92. PubMed ID: 14506069
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.
    Quattrone A; Gambardella A; Bono F; Aguglia U; Bolino A; Bruni AC; Montesi MP; Oliveri RL; Sabatelli M; Tamburrini O; Valentino P; Van Broeckhoven C; Zappia M
    Neurology; 1996 May; 46(5):1318-24. PubMed ID: 8628474
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Calf enlargement in hereditary motor and sensory neuropathy.
    De Visser M; Hoogendijk JE; Ongerboer BW; Verbeeten BJ
    Muscle Nerve; 1990 Jan; 13(1):40-6. PubMed ID: 2325700
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Coexistence of hereditary motor and sensory neuropathy type Ia and IgM paraproteinemic neuropathy.
    Gregory R; Thomas PK; King RH; Hallam PL; Malcolm S; Hughes RA; Harding AE
    Ann Neurol; 1993 Jun; 33(6):649-52. PubMed ID: 8498845
    [TBL] [Abstract][Full Text] [Related]  

  • 67. [Hereditary neuropathy with liability to pressure palsies in childhood].
    de las Cuevas I; Arteaga R; García A; Herranz JL
    Rev Neurol; 2000 Jul 1-15; 31(1):38-41. PubMed ID: 10948581
    [TBL] [Abstract][Full Text] [Related]  

  • 68. [A case of hereditary motor and sensory neuropathy with pyramidal tract sign, optic nerve atrophy and mental retardation].
    Adachi T; Imaoka K; Shirasawa A; Yamaguchi S; Kobayashi S
    Rinsho Shinkeigaku; 1998 Dec; 38(12):1037-41. PubMed ID: 10349345
    [TBL] [Abstract][Full Text] [Related]  

  • 69. X-linked dominant hereditary motor and sensory neuropathy.
    Hahn AF; Brown WF; Koopman WJ; Feasby TE
    Brain; 1990 Oct; 113 ( Pt 5)():1511-25. PubMed ID: 2245309
    [TBL] [Abstract][Full Text] [Related]  

  • 70. The phenotype of motor neuropathies associated with BSCL2 mutations is broader than Silver syndrome and distal HMN type V.
    Irobi J; Van den Bergh P; Merlini L; Verellen C; Van Maldergem L; Dierick I; Verpoorten N; Jordanova A; Windpassinger C; De Vriendt E; Van Gerwen V; Auer-Grumbach M; Wagner K; Timmerman V; De Jonghe P
    Brain; 2004 Sep; 127(Pt 9):2124-30. PubMed ID: 15242882
    [TBL] [Abstract][Full Text] [Related]  

  • 71. N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndrome.
    Rakocević-Stojanović V; Milić-Rasić V; Perić S; Baets J; Timmerman V; Dierick I; Pavlović S; De Jonghe P
    J Neurol Sci; 2010 Sep; 296(1-2):107-9. PubMed ID: 20598714
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene.
    Birouk N; Azzedine H; Dubourg O; Muriel MP; Benomar A; Hamadouche T; Maisonobe T; Ouazzani R; Brice A; Yahyaoui M; Chkili T; Le Guern E
    Arch Neurol; 2003 Apr; 60(4):598-604. PubMed ID: 12707075
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Hereditary sensory ataxic neuropathy associated with proximal muscle weakness in the lower extremities.
    Murakami T; Fukai Y; Rikimaru M; Henmi S; Ohsawa Y; Sunada Y
    J Neurol Sci; 2010 Apr; 291(1-2):121-3. PubMed ID: 20083254
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy.
    Plante-Bordeneuve V; Said G
    Muscle Nerve; 2002 Nov; 26(5):608-21. PubMed ID: 12402282
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Marked phenotypic variation in a family with a new myelin protein zero mutation.
    Szabo A; Züchner S; Siska E; Mechler F; Molnar MJ
    Neuromuscul Disord; 2005 Nov; 15(11):760-3. PubMed ID: 16198109
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entity.
    Sabatelli M; Mignogna T; Lippi G; Servidei S; Zollino M; Padua L; Lo Monaco M; De Armas L; Mereu ML; Tonali P
    Am J Med Genet; 1998 Jan; 75(3):309-13. PubMed ID: 9475604
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Hereditary neuropathy with liability to pressure palsies: electrophysiological and genetic study of a family with carpal tunnel syndrome as only clinical manifestation.
    Del Colle R; Fabrizi GM; Turazzini M; Cavallaro T; Silvestri M; Rizzuto N
    Neurol Sci; 2003 Jun; 24(2):57-60. PubMed ID: 12827539
    [TBL] [Abstract][Full Text] [Related]  

  • 78. The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V.
    Dubourg O; Azzedine H; Yaou RB; Pouget J; Barois A; Meininger V; Bouteiller D; Ruberg M; Brice A; LeGuern E
    Neurology; 2006 Jun; 66(11):1721-6. PubMed ID: 16769947
    [TBL] [Abstract][Full Text] [Related]  

  • 79. The application of nerve conduction and clinical studies to genetic counseling in hereditary motor and sensory neuropathy type I.
    Berciano J; Combarros O; Calleja J; Polo JM; Leno C
    Muscle Nerve; 1989 Apr; 12(4):302-6. PubMed ID: 2770783
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene.
    Sevilla T; Cuesta A; Chumillas MJ; Mayordomo F; Pedrola L; Palau F; Vílchez JJ
    Brain; 2003 Sep; 126(Pt 9):2023-33. PubMed ID: 12821518
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.