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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

NON-HYPERTROPHIC FAMILIAL NEUROPATHY ASSOCIATED WITH INTENTION TREMOR = NEUROPATHIE FAMILIALE NON HYPERTROPHIQUE ASSOCIEE A UN TREMBLEMENT INTENTIONNEL. UNE VARIETE DE MALADIE DE CHARCOT-MARIE-TOOTHDELWAIDE PJ; SCHOENEN J.1975; J. NEUROL. SCI.; NETHERL.; DA. 1975; VOL. 27; NO 1; PP. 59-69; BIBL. 1 P.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

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

VARIANTES CLINIQUES DE L'ATARIE FAMILIALE DE FRIEDREICHDEDIK GK.1975; KLIN. MED.; S.S.S.R.; DA. 1975; VOL. 53; NO 9; PP. 80-83; ABS. ANGL.; BIBL. 23 REF.Article

UN CASO DE ATROFIA PERONEA TIPO CHARCOT-MARIE-TOOTH CON TEMBLOR ESSENCIAL = UN CAS D'ATROPHIE PERONIERE TYPE CHARCOT-MARIE-TOOTH AVEC TREMBLEMENT ESSENTIELSALISACHS P.1975; MED. CLIN.; ESP.; DA. 1975; VOL. 65; NO 5; PP. 246-251; ABS. ANGL.; BIBL. 1 P. 1/2Article

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

ZUM BEGRIFF DER NEUROGENEN CLAUDICATION INTERMITTENS. UEBER EINE SELTENE FROM INTERMITTIERENDEN HINKENS BEI NEUROLOGISCHER SYSTEMERKRANKUNG. = LA NOTION DE CLAUDICATION INTERMITTENTE NEUROGENE. A PROPOS D'UNE FORME RARE DE BOITERIE INTERMITTENTE DANS UNE MALADIE DE SYSTEME NEUROLOGIQUEROSS A.1975; MUENCH. MED. WSCHR.; DTSCH.; DA. 1975; VOL. 117; NO 40; PP. 1609-1610; ABS. ANGL.; BIBL. 11 REF.Article

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

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

A FAMILY WITH CHARCOT-MARIE-TOOTH DISEASE AND LEBER'S OPTIC ATROPHY = UNE FAMILLE AVEC UNE MALADIE DE CHARCOT-MARIE-TOOTH ET ATROPHIE OPTIQUE DE LEBERMCLEOD JG; LOW PA; MORGAN JA et al.1975; PROC. AUSTRAL. ASS. NEUROLOGISTS; AUSTRAL.; DA. 1975; VOL. 12; PP. 23-25; BIBL. 18 REF.Article

GENETIC AND CLINICAL ASPECTS OF CHARCOT-MARIE-TOOTH'S DISEASE = ASPECTS GENETIQUES ET CLINIQUES DE LA MALADIE DE CHARCOT-MARIE-TOOTHSKRE H.1974; CLIN. GENET.; DENM.; DA. 1974; VOL. 6; NO 2; PP. 98-118; BIBL. 2 P.Article

EINE NEUE SIPPE MIT NEURALER MUSKELATROPHIE VOM TYP CHARCOT-MARIE-TOOTH = UNE NOUVELLE FAMILLE A CAS D'ATROPHIE MUSCULAIRE PROGRESSIVE DE TYPE CHARCOT-MARIE-TOOTHWAGNER A.1974; WISSENSCH. Z. ERNST MORITZ ARNDT-UNIV. GREIFSWALD, MATH.-NATURWISSENSCH. REIHE; DTSCH.; DA. 1974; VOL. 23; NO 2; PP. 227-236; BIBL. 24REF.Article

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

LA MALADIE DE CHARCOT-MARIE-TOOTHLAROCHE CHOLETTE A; BOUCHARD JP; GAGNE F et al.1974; VIE MED. CANADA FR.; CANADA; DA. 1974; VOL. 3; NO 11; PP. 1046-1054; ABS. ANGL.; BIBL. 17 REF.Article

ETUDE GENETIQUE D'UNE FAMILLE ATTEINTE DE MALADIE DE CHARCOT-MARIE-TOOTHGENCIK A; JAGR J; MATULOVA B et al.1974; CESKOSL. NEUROL. NEUROCHIR.; CESKOSL.; DA. 1974; VOL. 37; NO 5; PP. 316-320; ABS. RUSSE ANGL.; BIBL. 11 REF.Article

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

SEX-LINKED RECESSIVE INHERITANCE IN CHARCOT-MARIE-TOOTH DISEASE WITH PARTIAL CLINICAL MANIFESTATIONS IN FEMALE CARRIERSFRYNS JP; VAN DEN BERGHE H.1980; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1980; VOL. 55; NO 3; PP. 413-415; BIBL. 7 REF.Article

ENFERMEDAD DE CHARCOT-MARIE-TOOTH Y MIOCARDIOPATIA HIPERTROFICA = MALADIE DE CHARCOT-MARIE-TOOTH ET MYOCARDIOPATHIE HYPERTROPHIQUERODRIGUEZ CUARTERO A; LOPEZ LUQUE A; POMARES MORA J et al.1980; REV. CLIN. ESP.; ESP; DA. 1980; VOL. 156; NO 3; PP. 197-201; BIBL. 48 REF.Article

AUTOSOMAL RECESSIVE FORMS OF HEREDITARY MOTOR AND SENSORY NEUROPATHYHARDING AE; THOMAS PK.1980; J. NEUROL. NEUROSURG. PSYCHIATRY; ISSN 0022-3050; GBR; DA. 1980; VOL. 43; NO 8; PP. 669-678; BIBL. 28 REF.Article

BALANCING AS A CLINICAL TEST IN THE DIFFERENTIAL DIAGNOSIS OF SENSORY-MOTOR DISORDERSMAURITZ KH; DIETZ V; HALLER M et al.1980; J. NEUROL. NEUROSURG. PSYCHIATRY; GBR; DA. 1980; VOL. 43; NO 5; PP. 407-412; BIBL. 16 REF.Article

A PROPOS D'UNE OBSERVATION DE MALADIE DE CHARCOT AVEC PLEIOCYTOSE DU LIQUIDE CEPHALO-RACHIDIENPAGNY TROUSSARD JOSEPH.1979; ; FRA; PARIS: ETUDIANTS SERV.; DA. 1979; 16; 34-III P.: ILL.; 30 CM; BIBL. 3 P.; TH.: MED./PARIS 6/1979Thesis

HEREDITARY MOTOR AND SENSORY POLYNEUROPATHY (PERONEAL MUSCULAR ATROPHY = POLYNEUROPATHIE MOTRICE ET SENSORIELLE HEREDITAIRE (ATROPHIE MUSCULAIRE PERONIERE)THOMAS PK; CALNE DB; STEWART G et al.1974; ANN. HUM. GENET.; G.B.; DA. 1974; VOL. 38; NO 2; PP. 111-153; BIBL. 2P.1/2Article

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