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2. [Roussy-Levi disease (Study of a familial nucleus)]. Paolozzi C; Ammendola A; Bravaccio F; Tata MR; Volpe E; De Angelis G Acta Neurol (Napoli); 1977; 32(3):263-75. PubMed ID: 883520 [No Abstract] [Full Text] [Related]
3. [Difficult classification of a clinical form of osteochondrodystrophy associated with neurological disturbances of an extrapyramidal type. Clinical and biochemical study in 4 brothers]. Buscaino GA; Caruso G Acta Neurol (Napoli); 1968; 23(1):34-60. PubMed ID: 5739568 [No Abstract] [Full Text] [Related]
4. Lafora's disease--a distinct genetically determined form of Unverricht's syndrome. Yanoff M; Schwarz GA J Genet Hum; 1965 Sep; 14(2):235-44. PubMed ID: 5849253 [No Abstract] [Full Text] [Related]
5. Mast syndrome: a recessively inherited form of presenile dementia with motor disturbances. Cross HE Birth Defects Orig Artic Ser; 1971 Feb; 7(1):214-5. PubMed ID: 5173363 [No Abstract] [Full Text] [Related]
6. [On the position of hereditary areflectory dysstasia (Roussy and Lévy) in the group of heredodegenerative and systemic diseases of the central nervous system. With particular consideration of one family observation]. Heinroth H Dtsch Z Nervenheilkd; 1967; 191(1):10-21. PubMed ID: 6051944 [No Abstract] [Full Text] [Related]
7. A subacute progressive encephalopathy with mutism, hypokinesia, rigidity, and myoclonus. PALLIS CA; SPILLANE JD Q J Med; 1957 Jul; 26(103):349-73. PubMed ID: 13466002 [No Abstract] [Full Text] [Related]
8. A kinship of the Roussy-Levy syndrome: a clinical and electrophysiological study. Yudell A; Dyck PJ; Lambert EH Trans Am Neurol Assoc; 1964; 89():45-50. PubMed ID: 5828526 [No Abstract] [Full Text] [Related]
9. Superior intelligence in recessively inherited torsion dystonia. Eldridge R; Harlan A; Cooper IS; Riklan M Lancet; 1970 Jan; 1(7637):65-7. PubMed ID: 4188627 [No Abstract] [Full Text] [Related]
10. An unstable ring chromosome in a female infant with hypotonia, seizures, and retarded development. Atkins L; Sceery RT; Keenan ME J Med Genet; 1966 Jun; 3(2):134-8. PubMed ID: 5963207 [No Abstract] [Full Text] [Related]
11. MICU1 mutation: a genetic cause for a type of neuromuscular disease in children. Xu X Clin Genet; 2015 Apr; 87(4):327-8. PubMed ID: 25410274 [No Abstract] [Full Text] [Related]
12. [Nosographic and clinical aspects of the frontal syndrome]. Piccoli F; Lupo I; Fontana L Riv Neurol; 1981; 51(4):206-26. PubMed ID: 7031825 [No Abstract] [Full Text] [Related]
13. Familial paroxysmal dystonic choreoathetosis: a neurologic disorder simulating psychiatric illness. Walker ES Johns Hopkins Med J; 1981 Mar; 148(3):108-13. PubMed ID: 7206405 [TBL] [Abstract][Full Text] [Related]
14. [Hallervorden-Spatz disease in a brother and a sister (hereditary-familial fragility of the extrapyramidal apparatus)]. de Barsy T J Genet Hum; 1968 Jan; 16(3):41-7. PubMed ID: 5710711 [No Abstract] [Full Text] [Related]
15. [Myotonia-like deforming rigidity. (A new myo-oculo-skelatal disease sensitive to diphenylhydantoin)]. Laterza A; Paolella P; Valassi F Riv Otoneurooftalmol; 1967; 42(1):51-70. PubMed ID: 4971631 [No Abstract] [Full Text] [Related]
19. [Psychological development and progressive loss of movement in myopathic children (author's transl)]. Colin D; Lavenant J; Nurit JF Neuropsychiatr Enfance Adolesc; 1980; 28(1-2):51-8. PubMed ID: 7374926 [No Abstract] [Full Text] [Related]
20. [Adduction movement disorders of the finger]. Murota K; Nagao Y; Sato T; Imamura S Seikei Geka; 1970 Oct; 21(11):942-4. PubMed ID: 5528895 [No Abstract] [Full Text] [Related] [Next] [New Search]