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Journal Abstract Search
229 related items for PubMed ID: 9549516
41. [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 [Abstract] [Full Text] [Related]
42. Congenital cataracts facial dysmorphism neuropathy syndrome, a novel complex genetic disease in Balkan Gypsies: clinical and electrophysiological observations. Tournev I, Kalaydjieva L, Youl B, Ishpekova B, Guergueltcheva V, Kamenov O, Katzarova M, Kamenov Z, Raicheva-Terzieva M, King RH, Romanski K, Petkov R, Schmarov A, Dimitrova G, Popova N, Uzunova M, Milanov S, Petrova J, Petkov Y, Kolarov G, Aneva L, Radeva O, Thomas PK. Ann Neurol; 1999 Jun; 45(6):742-50. PubMed ID: 10360766 [Abstract] [Full Text] [Related]
43. [Acute idiopathic sensory neuropathy: a case report]. Werneck LC, Correa Neto Y, Scola RH. Arq Neuropsiquiatr; 1993 Sep; 51(3):389-94. PubMed ID: 8297247 [Abstract] [Full Text] [Related]
44. [A gait disorder caused by hereditary motor-sensory neuropathy]. Sauter R. Z Orthop Ihre Grenzgeb; 1990 Sep; 128(2):123-7. PubMed ID: 2140641 [Abstract] [Full Text] [Related]
45. [A juvenile case of chronic inflammatory demyelinating polyradiculoneuropathy with severe onion bulb-like change mimicking hereditary neuropathy]. Oda M, Udaka F, Kubori T, Oka N, Kameyama M. No To Shinkei; 1999 Dec; 51(12):1075-9. PubMed ID: 10654306 [Abstract] [Full Text] [Related]
46. A new variant of sensory ataxic neuropathy with autosomal dominant inheritance. van Dijk GW, Wokke JH, Oey PL, Franssen H, Ippel PF, Veldman H. Brain; 1995 Dec; 118 ( Pt 6)():1557-63. PubMed ID: 8595484 [Abstract] [Full Text] [Related]
47. Hereditary motor and sensory neuropathy type I and motor neuron disease. An unusual association. La Pia S, Valiani R, Vitolo S, Galdiero S, Rossi V, Santangelo R, Barbieri F. Acta Neurol (Napoli); 1989 Aug; 11(4):226-32. PubMed ID: 2801256 [Abstract] [Full Text] [Related]
48. [A case with hereditary motor and sensory neuropathy with multiple cranial nerves involvement]. Nakamura N, Oka N, Nakamura S, Akiguchi I, Kashii S. Rinsho Shinkeigaku; 1995 May; 35(5):516-20. PubMed ID: 7664521 [Abstract] [Full Text] [Related]
49. MRI of peripheral nerves and pathology of sural nerves in hereditary motor and sensory neuropathy type III. Tachi N, Kozuka N, Ohya K, Chiba S, Naganuma M. Neuroradiology; 1995 Aug; 37(6):496-9. PubMed ID: 7477868 [Abstract] [Full Text] [Related]
50. Intraoperative on-nerve nerve conduction study and conversion factor in the sural nerve. Oh SJ, Hemmi S, Kurokawa K, Hatanaka Y. Muscle Nerve; 2010 Sep; 42(3):373-8. PubMed ID: 20589887 [Abstract] [Full Text] [Related]
51. Hereditary motor and sensory neuropathy Lom type in a Serbian family. Dacković J, Keckarević-Marković M, Komazec Z, Rakocević-Stojanović V, Lavrnić D, Stević Z, Ribarić K, Romac S, Apostolski S. Acta Myol; 2008 Oct; 27(2):59-62. PubMed ID: 19364063 [Abstract] [Full Text] [Related]
52. Hereditary motor and sensory neuropathy with optic atrophy. Ultrastructural and morphometric observations on nerve fibers, mitochondria, and dense-cored vesicles. Sommer C, Schröder JM. Arch Neurol; 1989 Sep; 46(9):973-7. PubMed ID: 2775013 [Abstract] [Full Text] [Related]
53. Hypertrophic neuropathy: atypical appearances resulting from the combination of type I hereditary motor and sensory neuropathy and diabetes mellitus. Thomas PK, King RH, Bradley JL. Neuropathol Appl Neurobiol; 1997 Aug; 23(4):348-51. PubMed ID: 9292875 [Abstract] [Full Text] [Related]
56. Autosomal recessive hereditary sensory neuropathy with spastic paraplegia. Thomas PK, Misra VP, King RH, Muddle JR, Wroe S, Bhatia KP, Anderson M, Cabello A, Vilchez J, Wadia NH. Brain; 1994 Aug; 117 ( Pt 4)():651-9. PubMed ID: 7922454 [Abstract] [Full Text] [Related]
57. Hereditary neuropathy with liability to pressure palsies: a clinical and genetic study of a Taiwanese family. Tsai YT, Kuo HC, Chu CC, Lin KP, Huang CC. Chang Gung Med J; 2005 Jan; 28(1):56-63. PubMed ID: 15804150 [Abstract] [Full Text] [Related]