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Charcot-Marie-Tooth disease: study of large kinship with an intermediate formROSSI, A; PARADISO, C; CIONI, R et al.Journal of neurology. 1985, Vol 232, Num 2, pp 91-98, issn 0340-5354Article

Maladie de Charcot-Marie-Tooth et épilepsie = Charcot Marie Tooth disease and epilepsyTRIDON, P; BRICHET, B; RAVAILLE, G et al.Annales médicales de Nancy et de l'Est. 1983, Vol 22, pp 175-179, issn 0221-3796Article

Peroneal muscular atrophy with pyramidal featuresHARDING, A. E; THOMAS, P. K.Journal of neurology, neurosurgery and psychiatry. 1983, Vol 47, Num 2, pp 168-172, issn 0022-3050Article

A FAMILY WITH CHARCOT-MARIE-TOOTH'S DISEASE, SHOWING A PROBABLE X-LINKED INCOMPLETELY DOMINANT INHERITANCEISELIUS L; GRIMBY L.1982; HEREDITAS; ISSN 0018-0661; SWE; DA. 1982; VOL. 97; NO 1; PP. 157-158; BIBL. 8 REF.Article

DUREES D'EVOLUTION DE LA MALADIE DE CHARCOT (A PROPOS D'UNE SERIE DE 61 CAS)SEBON BERNARD.sd; FRA; DA. S.D.; 212; 75-IV P.; 30 CM; BIBL. 35 REF.; TH.: MED./PARIS 6/1978Thesis

HEREDITARY MOTOR SENSORY NEUROPATHIES IN CHILDHOODROSSI LN; LUETSCHG J; MEIER C et al.1983; DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY; ISSN 0012-1622; GBR; DA. 1983; VOL. 25; NO 1; PP. 19-31; ABS. FRE/GER/SPA; BIBL. 1 P.Article

LES ATROPHIES PERONIERES ET LA MALADIE DE CHARCOT-MARIE-TOOTHSERRATRICE G.1982; MED. HYG.; ISSN 0025-6749; CHE; DA. 1982; VOL. 40; NO 1486; PP. 3381-3386; 5 P.; BIBL. 10 REF.Article

MALADIE DE CHARCOT MARIE TOOTHKRSTIC S; VIDAKOVIC Z; IGNJATOVIC M et al.1976; NEUROPSIHIJATRIJA; JUGOSL.; DA. 1976; VOL. 24; NO 1-4; PP. 121-128; ABS. ANGL.; BIBL. 17 REF.Article

Respiratory muscle dysfunction in hereditary motor sensory neuropathy, type IEICHACKER, P. Q; SPIRO, A; SHERMAN, M et al.Archives of internal medicine (1960). 1988, Vol 148, Num 8, pp 1739-1740, issn 0003-9926Article

DISTAL AND SCALPULOPERONEAL DISTRIBUTIONS OF MUSCLE INVOLVEMENT OCCURING WITHIN A FAMILY WITH TYPE I HEREDITARY MOTOR AND SENSORY NEUROPATHYHARDING AE; THOMAS PK.1980; J. NEUROL.; DEU; DA. 1980; VOL. 224; NO 1; PP. 17-23; ABS. GER; BIBL. 15 REF.Article

HEREDITARY MOTOR AND SENSORY NEUROPATHIES IN SWEDISH CHILDREN. III: DE- AND REMYELINATING TYPE IN 10 SPORADIC CASESHAGBERG B; WESTERBERG B; HAGNE I et al.1983; ACTA PAEDIATRICA SCANDINAVICA; ISSN 0001-656X; SWE; DA. 1983; VOL. 72; NO 4; PP. 537-544; BIBL. 27 REF.Article

HEREDITARY MOTOR AND SENSORY NEUROPATHY. REPLYBIRD TD; HARDLING AE; THOMAS PK et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 5; PP. 399; BIBL. 5 REF.Article

HLA IN CHARCOT-MARIE-TOOTH DISEASEWILLIAMS LL.1980; ANN. NEUROL.; ISSN 0364-5134; USA; DA. 1980; VOL. 8; NO 4; PP. 452; BIBL. 4 REF.Article

PATTERN REVERSAL VISUAL EVOKED POTENTIALS. STUDIES IN CHARCOT-MARIE-TOOTH HEREDITARY NEUROPATHYBIRD TD; GRIEP E.1981; ARCH. NEUROL. (CHIC.); ISSN 0003-9942; USA; DA. 1981; VOL. 38; NO 12; PP. 739-741; BIBL. 21 REF.Article

GENETIC ASPECTS OF HEREDITARY MOTOR AND SENSORY NEUROPATHY (TYPES I AND II)HARDING AE; THOMAS PK.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 8; PP. 329-336; BIBL. 53 REF.Article

DU POLYMORPHISME DE L'AMYOTROPHIE NEURONALE DE CHARCOT-MARIE-TOOTH CHEZ LES JUMEAUX MONOZYPOTESPOPOV'YAN MD; DUBINSKAYA E EH; AGEEVA TS et al.1977; ZH. NEVROPATOL. PSIKHIATR. S.S. KORSAKOVA; S.S.S.R.; DA. 1977; VOL. 77; NO 10; PP. 1446-1448; ABS. ANGL.; BIBL. 6 REF.Article

CLINICAL AND ELECTRODIAGNOSTIC FEATURES OF CHARCOT-MARIE-TOOTH SYNDROMEBRUST JCM; LOVELACE RE; DEVI S et al.1978; ACTA NEUROL. SCAND., SUPPL.; DNK; DA. 1978; VOL. 58; NO 68; PP. 1-142; BIBL. DISSEM.Serial Issue

L'ELECTROMYOGRAPHIE DANS LA MALADIE DE CHARCOT-MARIEZUMSTEIN V; SCHNEIDER C.1982; SCHWEIZ. ARCH. NEUROL. NEUROCHIR. PSYCHIATR.; ISSN 0036-7273; CHE; DA. 1982; VOL. 130; NO 2; PP. 297-307; ABS. GER; BIBL. 13 REF.Article

ENFERMEDAD DE CHARCOT-MARIE-TOOTH. UNA OBSERVACION A EDAD TEMPRANA. = MALADIE DE CHARCOT-MARIE-TOOTH. UNE OBSERVATION A UN AGE PRECOCECASTRO M; CABANAS R; ALVEZ E et al.1977; REV. ESP. PEDIATR.; ESP.; DA. 1977; VOL. 33; NO 198; PP. 633-640; ABS. ANGL.; BIBL. 1 P. 1/2Article

HEREDITARY MOTOR AND SENSORY NEUROPATHIES IN SWEDISH CHILDREN. I: PREVALENCE AND DISTRIBUTION BY DISABILITY GROUPSHAGBERG B; WESTERBERG B.1983; ACTA PAEDIATRICA SCANDINAVICA; ISSN 0001-656X; SWE; DA. 1983; VOL. 72; NO 3; PP. 379-383; BIBL. 13 REF.Article

Pathophysiology of Charcot-Marie-Tooth diseaseMANN, R. A; MISSIRIAN, J.Clinical orthopaedics and related research. 1988, Num 234, pp 221-228, issn 0009-921XArticle

The natural history of Charcot-Marie-Tooth type 1A in adults: a 5-year follow-up studyVERHAMME, Camiel; VAN SCHAIK, Ivo N; KOELMAN, Johannes H. T. M et al.Brain. 2009, Vol 132, pp 3252-3262, issn 0006-8950, 11 p., 12Article

HEREDITARY DISTAL SPINAL MUSCULAR ATROPHY: A REPORT ON 34 CASES AND A REVIEW OF THE LITERATUREHARDING AE; THOMAS PK.1980; J. NEUROL. SCI.; NLD; DA. 1980; VOL. 45; NO 2-3; PP. 337-348; BIBL. 26 REF.Article

PATTERN SHIFT VISUAL EVOKED POTENTIALS IN CHARCOT-MARIE-TOOTH DISEASE, HMSN TYPE ITACKMANN W; RADU EW.1980; J. NEUROL.; DEU; DA. 1980; VOL. 224; NO 1; PP. 71-74; ABS. GER; BIBL. 20 REF.Article