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Journal Abstract Search
233 related items for PubMed ID: 5715887
1. [Diagnosis and nosographic classification of muscular hypotonia in infancy]. Cazzato G. Riv Sper Freniatr Med Leg Alien Ment; 1968 Apr 30; 92(2):525-51. PubMed ID: 5715887 [No Abstract] [Full Text] [Related]
2. [Clinical-genetic classification of muscular dystrophies]. López de Munain A, Andoni Urtizberea J. Med Clin (Barc); 1998 Sep 05; 111(6):226-35. PubMed ID: 9789230 [No Abstract] [Full Text] [Related]
3. [Current views on the diagnosis, etiology and genetics of the most frequent non-metabolic congenital myopathies]. Herrmann V. Padiatr Grenzgeb; 1983 Sep 05; 22(1):27-45. PubMed ID: 6866527 [No Abstract] [Full Text] [Related]
4. [Histological and histochemical diagnosis of muscular diseases in childhood]. Minetti C. Minerva Pediatr; 1982 Nov 30; 34(22):969-76. PubMed ID: 6759914 [No Abstract] [Full Text] [Related]
5. [Fundamentals and clinical significance of electromyography]. Buchthal F. Verh Dtsch Ges Inn Med; 1965 Nov 30; 71():139-60. PubMed ID: 5877614 [No Abstract] [Full Text] [Related]
6. [Diabetic amyotrophy]. Hirata Y, Toyoda T. Naika; 1971 Apr 30; 27(4):737-41. PubMed ID: 5553512 [No Abstract] [Full Text] [Related]
7. [Value of determination of glycogen and some of its degradation products in differential diagnosis of primary and secondary muscular diseases in children]. Anczykowa A. Folia Med Cracov; 1967 Apr 30; 9(2):207-31. PubMed ID: 6081895 [No Abstract] [Full Text] [Related]
8. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood. Gamstorp I. Birth Defects Orig Artic Ser; 1971 Feb 30; 7(2):72-81. PubMed ID: 5173129 [Abstract] [Full Text] [Related]
9. [For the anatomo-clinical diagnosis of primary muscular dystrophy of neonatal onset: apropos of a case]. Bruni G, Zalla PG. Arch De Vecchi Anat Patol; 1968 Mar 30; 51(1):435-45. PubMed ID: 5737308 [No Abstract] [Full Text] [Related]
10. [Malate dehydrogenase activity in children with myopathy]. Gil'manov VKh. Zh Nevropatol Psikhiatr Im S S Korsakova; 1973 Mar 30; 73(6):829-31. PubMed ID: 4753593 [No Abstract] [Full Text] [Related]
16. Electromyographic characteristics of congenital and early onset motor unit diseases. Fowler WM, Taylor RG, Munsat TL. Arch Phys Med Rehabil; 1971 Aug 05; 52(8):343-61. PubMed ID: 5284447 [No Abstract] [Full Text] [Related]
17. [The hypotonic infant: diagnostic problems. Attempted electromyographic, clinical, biochemical and anatomical classification of neuromyopathies of infants and young children]. Turner M, Garcia Villanueva G. Arch Argent Pediatr; 1966 Aug 05; 63(7):283-92. PubMed ID: 6011344 [No Abstract] [Full Text] [Related]
18. [Hypotonias in newborn and older infants]. Hennequet A. Ann Pediatr (Paris); 1967 Aug 05; 14(6):521-3. PubMed ID: 5618050 [No Abstract] [Full Text] [Related]
19. [Electrodiagnosis and clinical picture of myopathies]. Huffmann G. Z Allgemeinmed; 1974 Jan 31; 50(3):135-41. PubMed ID: 4826221 [No Abstract] [Full Text] [Related]
20. [Errors in the diagnosis of progressive muscular dystrophy and spinal muscular atrophy]. Parnitzke C, Hagen EM. Z Arztl Fortbild (Jena); 1981 Jul 01; 75(13):577-81. PubMed ID: 7314671 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]