Über den Wert mechanographischer Untersuchungen in der neuro-muskulären Funktionsdiagnostik = Valeur de la mécanographie pour le diagnostic fonctionnel neuromusculaire = The value of mecanography for neuromuscular functionnal diagnosticWAGNER, A; ZETT, L.Psychiatrie, Neurologie und medizinische Psychologie. 1984, Vol 36, Num 3, pp 130-139, issn 0033-2739Article

WEAKNESS IN MYOTONIC SYNDROMES.WILES CM; EDWARDS RHT.1977; LANCET; G.B.; DA. 1977; NO 8038; PP. 598-601; BIBL. 56 REF.Article

Myotonia congenita : A successful response to carbamazepineSAVITHA, M. R; KRISHNAMURTHY, B; HYDERI, Abbas et al.Indian journal of pediatrics. 2006, Vol 73, Num 5, pp 431-433, issn 0019-5456, 3 p.Article

Myotonia congenita: Novel mutations in CLCN1 gene and functional characterizations in Italian patientsULZI, Gianna; LECCHI, Marzia; D'ANGELO, Grazia et al.Journal of the neurological sciences. 2012, Vol 318, Num 1-2, pp 65-71, issn 0022-510X, 7 p.Article

A NOVEL CLCN1 MUTATION (G1652A) CAUSING A MILD PHENOTYPE OF THOMSEN DISEASEKUMAR, Kishore R; NG, Karl; VANDEBONA, Himesha et al.Muscle & nerve. 2010, Vol 41, Num 3, pp 412-415, issn 0148-639X, 4 p.Article

Novel mutations at carboxyl terminus of CIC-1 channel in myotonia congenitaKUO, H.-C; HSIAO, K.-M; CHANG, L.-I et al.Acta neurologica scandinavica. 2006, Vol 113, Num 5, pp 342-346, issn 0001-6314, 5 p.Article

Myotonia, periodic paramysis and myopathyWINTZEN, A. R.Clinical neurology and neurosurgery. 1992, Vol 94, pp S25-S27, issn 0303-8467, SUPConference Paper

Lithium-induced improvement of myotoniaGERST, J. W; BRUMBACK, R. A; STATON, R. D et al.Journal of neurology, neurosurgery and psychiatry. 1984, Vol 47, Num 9, pp 1044-1046, issn 0022-3050Article

MYOTONIC DYSTROPHY1981; DEU. NEUROL.; ISSN 0166-5960; NLD; DA. 1981; VOL. 5; PP. 3-78; BIBL. DISSEM.Conference Paper

LA MALADIE DE STEINERT: A PROPOS DE 123 CASAUDRY CHABOUD D; BADY B.1981; LYON MED.; ISSN 0024-7790; FRA; DA. 1981; VOL. 247; NO 17; PP. 255-263; ABS. ENG; BIBL. 50 REF.Article

MYOTONIA CONGENITA (THOMSEN'S DISEASE): EARLY DIAGNOSIS IN INFANCYHAREL S; CHUI LA; SHAPIRA Y et al.1979; ACTA PAEDIATR. SCAND.; SWE; DA. 1979; VOL. 68; NO 2; PP. 225-227; BIBL. 12 REF.Article

MYOTONIC DYSTROPHYHARPER PS.1979; MAJOR PROBL. NEUROL.; GBR; DA. 1979; VOL. 9; 343 P.; BIBL. DISSEM.Serial Issue

LA MALADIE DE STEINERT INFANTILE. A PROPOS DE TROIS OBSERVATIONSGIROUD MAURICE.1979; ; FRA; DA. 1979; 136; 180 P.: ILL.; 30 CM; H.T. 1; BIBL. 135 REF.; TH.: MED./DIJON/1979Thesis

MYOTONIES, PARAMYOTONIES ET PSEUDOMYOTONIESGASTAUT JL.1979; VIE MED.; FRA; DA. 1979; VOL. 60; NO 26; PP. 2271-2279; ( 5 P.); BIBL. 11 REF.Article

HETEROZYGOTE MANIFESTATION IN RECESSIVE GENERALIZED MYOTONIABECKER PE.1978; HUM. GENET.; DEU; DA. 1978; VOL. 46; NO 3; PP. 325-329; BIBL. 7 REF.Article

MYOTONIA IN CENTRONUCLEAR MYOPATHYGIL PERALTA A; RAFEL E; BAUTISTA J et al.1978; J. NEUROL. NEUROSURG. PSYCHIATRY; GBR; DA. 1978; VOL. 41; NO 12; PP. 1102-1108; BIBL. 27 REF.Article

ERGEBNISSE ELEKTROMYOGRAPHISCHER UND MECHANOGRAPHISCHER UNTERSUCHUNGEN BEI MYOTONIA CONGENITA = RESULTATS DES EXPLORATIONS ELECTROMYOGRAPHIQUES ET MECANOGRAPHIQUES DANS LA MYOTONIE CONGENITALEWAGNER A; ZETT L.1982; EEG-EMG; ISSN 0012-7590; DEU; DA. 1982; VOL. 13; NO 1; PP. 14-21; ABS. ENG; BIBL. 43 REF.Article

LA MALADIE DE THOMSEN.DEBRAND J; SAINMONT C; NOIR A et al.1976; REV. INTERNATION. PEDIATR.; FR.; DA. 1976; NO 65; PP. 5-17 (11P.); BIBL. 32 REF.Article

LA MYOTONIE CONGENITALE OU MALADIE DE THOMSEN CHEZ L'ENFANT. A PROPOS D'UNE OBSERVATION.MARANDIAN MH; ASKARI H; KABIRI M et al.1976; PEDIATRIE; FR.; DA. 1976; VOL. 31; NO 5; PP. 505-509; ABS. ANGL.; BIBL. 13 REF.Article

MYOTONIC DYSTROPHY AND HYPERTHYROIDISMOKUNO T; MORI K; FUROMI K et al.1981; NEUROLOGY; ISSN 0028-3878; USA; DA. 1981; VOL. 31; NO 1; PP. 91-93; BIBL. 14 REF.Article

20,25-DIAZACHOLESTEROL MYOTONIA: AN ELECTROPHYSIOLOGICAL STUDYFURMAN RE; BARCHI RL.1981; ANN. NEUROL.; ISSN 0364-5134; USA; DA. 1981; VOL. 10; NO 3; PP. 251-260; BIBL. 29 REF.Article

ESTUDIO CLINICO DE 8 FAMILIAS CON DISTINTOS MIEMBROS AFECTADOS DE DISTROFIA MIOTONICA TIPO CURSCHMANN-STEINERT = ETUDE CLINIQUE DE 8 FAMILLES AVEC DIVERS MEMBRES ATTEINTS DE DYSTROPHIE MYOTONIQUE TYPE CURSCHMANN-STEINERTMORALES ASIN F; MOSTACERO MIGUEL E; GARCIA ALVAREZ F et al.1980; REV. CLIN. ESP.; ESP; DA. 1980; VOL. 157; NO 5; PP. 313-318; ABS. ENG/GER/FRE; BIBL. 28 REF.Article

MALADIE DE STEINERT A REVELATION NEO-NATALE: A PROPOS DE DEUX OBSERVATIONSLALANNE ANNE MARIE.1978; ; FRA; BORDEAUX: BERGERET; DA. 1978; 143; 73 P.: ILL.-PL.; 24,5 CM; BIBL. 85 REF.; TH.: MED./BORDEAUX 2/1978Thesis

MALADIE DE STEINERT ET GROSSESSESADOUL G; BEURET T; LEWIN D et al.1978; SEM. HOP.; FRA; DA. 1978; VOL. 54; NO 21-24; PP. 758-761; ABS. ENG; BIBL. 20 REF.Article

SENSITIVITY OF SKELETAL MUSCLE TO 20, 25-DIAZACHOLESTEROL-INDUCED MYOTONIA REQUIRES NORMAL INNERVATIOND'ALONZO AJ; MCARDLE JJ; ARGENTIER TM et al.1982; EXP. NEUROL.; ISSN 0014-4886; USA; DA. 1982; VOL. 75; NO 2; PP. 466-475; BIBL. 27 REF.Article