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30. [Significance of alpha l-antitrypsin deficiency in chronic bronchopneumopathies]. Di Blasi S; Pintacuda S Folia Med (Napoli); 1969 Aug; 52(8):473-86. PubMed ID: 4990605 [No Abstract] [Full Text] [Related]
31. [Molecular analysis of pulmonary risk genes. Relevance for clinical research, diagnosis and therapy]. Poller WC; Faber JP Med Klin (Munich); 1993 Apr; 88(4):212-30. PubMed ID: 8492776 [No Abstract] [Full Text] [Related]
32. Hematological abnormalities in inborn errors of metabolism--how frequent are they? The Cretan experience. Evangeliou A; Dafnis E; Perdikoyanni C; Spilioti M; Lionis C; Kalmanti M Pediatr Hematol Oncol; 2002 Dec; 19(8):581-5. PubMed ID: 12487834 [TBL] [Abstract][Full Text] [Related]
33. Is there a relationship between inborn errors of metabolism and extensive mongolian spots? Mendez HM; Pinto LI; Paskulin GA; Ricachnevsky N Am J Med Genet; 1993 Sep; 47(4):456-7. PubMed ID: 8256803 [TBL] [Abstract][Full Text] [Related]
34. [Macular degeneration in hereditary metabolic diseases in children (inborn errors of metabolism)]. Stanescu-Segal B; Evrard P Bull Soc Belge Ophtalmol; 1984-1985; 212():109-15. PubMed ID: 6545872 [No Abstract] [Full Text] [Related]
37. Osteoporosis in children with neuromuscular diseases and inborn errors of metabolism. Plotkin H; Sueiro R Minerva Pediatr; 2007 Apr; 59(2):129-35. PubMed ID: 17404563 [TBL] [Abstract][Full Text] [Related]