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3. The future of the 'floppy infant': a follow-up study of 133 patients. PAINE RS Dev Med Child Neurol; 1963 Apr; 5():115-24. PubMed ID: 13941123 [No Abstract] [Full Text] [Related]
4. ELECTROMYOGRAM IN THE DIFFERENTIAL DIAGNOSIS OF THE "FLOPPY" INFANT. MARINACCI AA Bull Los Angel Neuro Soc; 1964 Jun; 29():70-5. PubMed ID: 14169954 [No Abstract] [Full Text] [Related]
5. [Muscle diseases in children: with special reference to progressive muscular dystrophy, amyotonia, myohypertonia and myoasthenia]. CORTESE-VERROTTI I Pediatria (Napoli); 1956; 64(2):341-7. PubMed ID: 13335311 [No Abstract] [Full Text] [Related]
6. [Familial occurrence of congenital cranial synostoses associated with Oppenheim's myatonia congenita]. STRAHM A Zentralbl Gynakol; 1953; 75(16):630-3. PubMed ID: 13091258 [No Abstract] [Full Text] [Related]
7. [ELECTROMYOGRAPHIC INVESTIGATIONS IN MYELO-MUSCULAR DYSPLASIAS IN CHILDHOOD]. BOTTONE E; CHECCUCCI A; VACCARONE A Minerva Pediatr; 1964 Mar; 16():378-86. PubMed ID: 14143190 [No Abstract] [Full Text] [Related]
15. Muscular hypotonia in infancy; diagnosis and differentiation. ZELLWEGER HU; SMITH JW; CUSMINSKY M Rev Can Biol; 1962; 21():599-612. PubMed ID: 14003443 [No Abstract] [Full Text] [Related]
16. [Case of congenital myopathy with dolichostenomelia]. STEGAGNO GA; COLETTA M Arch Ital Pediatr Pueric; 1955; 17(6):475-503. PubMed ID: 13303730 [No Abstract] [Full Text] [Related]
17. [DEVELOPMENTAL SYMPTOMATOLOGY OF SOME MOTOR SYNDROMES DURING INFANCY]. LESNY I Folia Clin Int (Barc); 1963 Oct; 13():471-81. PubMed ID: 14103473 [No Abstract] [Full Text] [Related]
18. The relationship between progressive muscular atrophy of spinal origin and amyotonia congenita. AREY JB; BAIRD HW AMA Am J Dis Child; 1953 Nov; 86(5):619-20; discussion, 620-1. PubMed ID: 13103782 [No Abstract] [Full Text] [Related]
19. [Torticollis ex amyotonia congenita]. DEZYNA M Chir Narzadow Ruchu Ortop Pol; 1957; 22(1):49-51. PubMed ID: 13473007 [No Abstract] [Full Text] [Related]
20. [Follow-up examination of children with spinal muscular atrophy of the Werdning-Hoffmann type; at the same time a critical contribution to the problem of amyotonia congenita Oppenheim]. KIRCHHOF JK; MULLER F Nervenarzt; 1958 Apr; 29(4):158-67. PubMed ID: 13552903 [No Abstract] [Full Text] [Related] [Next] [New Search]