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4. [Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)--clinical features and the findings of nerve pathology]. Tachi N; Hosoya S; Sasaki K; Watanabe M; Nagaoka M; Wakai S; Kameda K; Minami R No To Hattatsu; 1988 May; 20(3):211-6. PubMed ID: 3164619 [No Abstract] [Full Text] [Related]
5. Hereditary sensory neuropathy: a case with pain and temperature dissociation. O'Brien B; Jackson R; Tang-Wai R; Lewis AJ; Atack EA Can J Neurol Sci; 1980 Feb; 7(1):73-6. PubMed ID: 6930314 [TBL] [Abstract][Full Text] [Related]
7. [Neuromuscular diseases in childhood and adolescence]. Karch D Offentl Gesundheitswes; 1988; 50(8-9):474-9. PubMed ID: 2972963 [No Abstract] [Full Text] [Related]
8. [Monogenic inheritance: nervous system and neuromuscular diseases]. Moser H Ther Umsch; 1986 Dec; 43(12):893-906. PubMed ID: 3824260 [No Abstract] [Full Text] [Related]
9. Peripheral motor neuropathy associated with autonomic dysfunction in two sisters: new hereditary syndrome? Lisker R; García-Ramos G; de la Rosa-Laris C; Díaz-Mitoma F Am J Med Genet; 1981; 9(3):255-9. PubMed ID: 7282784 [TBL] [Abstract][Full Text] [Related]
10. [Molecular genetics of hereditary polyneuropathies]. Fernández Alvarez E An Esp Pediatr; 1999 Nov; 51(5):456-60. PubMed ID: 10652794 [No Abstract] [Full Text] [Related]
11. Disease mechanisms in hereditary sensory and autonomic neuropathies. Verpoorten N; De Jonghe P; Timmerman V Neurobiol Dis; 2006 Feb; 21(2):247-55. PubMed ID: 16183296 [TBL] [Abstract][Full Text] [Related]
12. Pathophysiology inferred from electrodiagnostic nerve tests and classification of polyneuropathies. Suggested guidelines. Tankisi H; Pugdahl K; Fuglsang-Frederiksen A; Johnsen B; de Carvalho M; Fawcett PR; Labarre-Vila A; Liguori R; Nix WA; Schofield IS; Clin Neurophysiol; 2005 Jul; 116(7):1571-80. PubMed ID: 15907395 [TBL] [Abstract][Full Text] [Related]
13. Late-onset hereditary sensory neuropathy type I due to SPTLC1 mutation: autopsy findings. Lindahl AJ; Lhatoo SD; Campbell MJ; Nicholson G; Love S Clin Neurol Neurosurg; 2006 Dec; 108(8):780-3. PubMed ID: 16271825 [TBL] [Abstract][Full Text] [Related]
14. Conduction block in hereditary neuropathy with susceptibility to pressure palsies. Sellman MS; Mayer RF Muscle Nerve; 1987 Sep; 10(7):621-5. PubMed ID: 3477693 [TBL] [Abstract][Full Text] [Related]
15. [Contribution of neuromuscular biopsy in cardiovascular diseases]. Mussini JM; Guillemot A; Mussini-Montpellier J Ann Cardiol Angeiol (Paris); 1979 Nov; 28(6):377-83. PubMed ID: 44823 [No Abstract] [Full Text] [Related]
16. [Autoantibodies in nervous system diseases]. Humbel RL; Schmit P; Gilson G Bull Soc Sci Med Grand Duche Luxemb; 1996; 133(1):13-24. PubMed ID: 8964104 [No Abstract] [Full Text] [Related]
17. [Tomaculous neuropathy. A histopathological study and electroclinical correlates in 10 cases]. Pellissier JF; Pouget J; de Victor B; Serratrice G; Toga M Rev Neurol (Paris); 1987; 143(4):263-78. PubMed ID: 3476973 [TBL] [Abstract][Full Text] [Related]
18. [Hereditary neuromuscular diseases in paediatrics. Our experience over the last 14 years]. López-Pisón J; Rebage V; Baldellou-Vázquez A; Capablo-Liesa JL; Colomer J; Calvo MT; Sáenz de Cabezón A; Alfaro-Torres J; del Agua C; Bestué M; Peña-Segura JL Rev Neurol; 2005 Aug 1-15; 41(3):145-50. PubMed ID: 16047297 [TBL] [Abstract][Full Text] [Related]