Familiar myoclonus-renal failure syndrome;Familiäres myoklonus-niereninsuffizienz-syndrom

Nervenarzt

Volumn 72, Issue 8, 2001, Pages 636-640

  Rothdach, A J ^a   Dietl, T ^a   Kumpfel T ^a   Gottschalk, M ^a   Schumann, E M ^a   Trenkwalder, C ^a  

^a MAX PLANCK INSTITUTE OF PSYCHIATRY   (Germany)

Author keywords

Autosomal recessive inheritance; Demyelinizing polyneuropathy; Epilepsy; Kidney insufficiency; Mixed polyneuropathy; Myoclonus; Zerebellar symptomatology

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CEREBELLUM DISEASE; CLINICAL FEATURE; DIALYSIS; DISEASE COURSE; EPILEPSY; EUROPE; FAMILIAL DISEASE; FEMALE; GRAND MAL SEIZURE; HUMAN; KIDNEY BIOPSY; KIDNEY FAILURE; MALE; MYOCLONUS; NEPHRITIS; POLYNEUROPATHY; SYNDROME;

ADOLESCENT; ADULT; CEREBELLAR DISEASES; CHROMOSOME ABERRATIONS; ELECTROENCEPHALOGRAPHY; EPILEPSY; EPILEPSY, TONIC-CLONIC; FEMALE; GENES, RECESSIVE; HUMANS; KIDNEY FAILURE, CHRONIC; MALE; MYOCLONUS; NEUROLOGIC EXAMINATION; PEDIGREE; SYNDROME;

EID: 0034894241     PISSN: 00282804     EISSN: None     Source Type: Journal    
DOI: 10.1007/s001150170065     Document Type: Article

References (8)

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