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4. Investigations of 3 cases of a newly recognized familial, congenital myasthenic syndrome. Engel AG; Lambert EH; Mulder DM; Torres CF; Sahashi K; Bertorini TE; Whitaker JN Trans Am Neurol Assoc; 1979; 104():8-12. PubMed ID: 233333 [No Abstract] [Full Text] [Related]
5. [Translocation of group D chromosomes in a child with a congenital syndrome of neuromyodysplasia and mental retardation]. Traczyńska-Kubin H; Czerski P; Rogóyski A; Stolarska A Pediatr Pol; 1975 Dec; 50(12):1485-7. PubMed ID: 1196721 [No Abstract] [Full Text] [Related]
6. [3 examples of fetal genetic neuromuscular disorders which lead to hydramnion]. Teeuw AH; Barth PG; van Sonderen L; Zondervan HA Ned Tijdschr Geneeskd; 1993 May; 137(18):908-13. PubMed ID: 8492834 [TBL] [Abstract][Full Text] [Related]
7. [Hereditary neuromuscular diseases in paediatrics. Our experience over the last 14 years]. López-Pisón J; Rebage V; Baldellou-Vázquez A; Capablo-Liesa JL; Colomer J; Calvo MT; Sáenz de Cabezón A; Alfaro-Torres J; del Agua C; Bestué M; Peña-Segura JL Rev Neurol; 2005 Aug 1-15; 41(3):145-50. PubMed ID: 16047297 [TBL] [Abstract][Full Text] [Related]
8. Mallory body-like inclusions in a hereditary congenital neuromuscular disease. Fidzianska A; Goebel HH; Osborn M; Lenard HG; Osse G; Langenbeck U Muscle Nerve; 1983; 6(3):195-200. PubMed ID: 6343859 [TBL] [Abstract][Full Text] [Related]
9. Congenital disorders of neuromuscular transmission. Engel AG Semin Neurol; 1990 Mar; 10(1):12-26. PubMed ID: 2161125 [No Abstract] [Full Text] [Related]
15. Molecular diagnosis of inheritable neuromuscular disorders. Part II: Application of genetic testing in neuromuscular disease. Greenberg SA; Walsh RJ Muscle Nerve; 2005 Apr; 31(4):431-51. PubMed ID: 15704143 [TBL] [Abstract][Full Text] [Related]
16. Rehabilitation of children and adults who have neuromuscular diseases. Hornyak JE; Pangilinan PH Phys Med Rehabil Clin N Am; 2007 Nov; 18(4):883-97, vii-viii. PubMed ID: 17967367 [TBL] [Abstract][Full Text] [Related]
17. [Organization of therapeutic aid to patients with hereditary neuromuscular diseases]. Kalinin VA; Temin PA; Arkhipov BA; Zavadenko NN Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(12):26-9. PubMed ID: 2633564 [TBL] [Abstract][Full Text] [Related]
20. [Congenital neuromuscular disease with uniform type 1 fiber complicated by brain atrophy: a case report]. Li XH; Zhang J; Cui XE Zhongguo Dang Dai Er Ke Za Zhi; 2010 Jun; 12(6):496-8. PubMed ID: 20540866 [No Abstract] [Full Text] [Related] [Next] [New Search]