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63. Some biochemical aspects of scoliosis and their pathogenetic significance. Balaba TY Reconstr Surg Traumatol; 1972; 13():191-209. PubMed ID: 5070996 [No Abstract] [Full Text] [Related]
72. [A genetic muscular creatine phosphokinase abnormality in a family with malignant hyperpyrexia]. Zsigmond EK; Starkweather WH; Duboff GS; Flyn K Rev Bras Anestesiol; 1971; 21(3):265-76. PubMed ID: 5138487 [No Abstract] [Full Text] [Related]
73. [Metabolic encephalopathy and nephropathy caused by congenital hyperuricemia]. Polonovski C; Laplane R; Graveleau D; Baheux G; Sicre MC Bull Mem Soc Med Hop Paris; 1966 Jun; 117(9):799-812. PubMed ID: 5927100 [No Abstract] [Full Text] [Related]
74. [Maculopathy in hereditary metabolic diseases]. Stănescu-Segall B Oftalmologia; 1996; 40(3):261-3. PubMed ID: 8962852 [TBL] [Abstract][Full Text] [Related]
75. Renal replacement therapy in the treatment of confirmed or suspected inborn errors of metabolism. McBryde KD; Kershaw DB; Bunchman TE; Maxvold NJ; Mottes TA; Kudelka TL; Brophy PD J Pediatr; 2006 Jun; 148(6):770-8. PubMed ID: 16769384 [TBL] [Abstract][Full Text] [Related]
76. [Metabolically induced epileptic seizures in childhood]. Vassella F Schweiz Rundsch Med Prax; 1983 Jun; 72(24):827-31. PubMed ID: 6878165 [No Abstract] [Full Text] [Related]
77. [On the symptomatology of mental retardation]. Suchenwirth R Med Monatsschr; 1969 Jan; 23(1):8-13. PubMed ID: 5766687 [No Abstract] [Full Text] [Related]
78. [Selective congenital malabsorption of vitamin B 12 with proteinuria]. Gräsbeck R; Kvist G Minerva Med; 1967 Oct; 58(82):3488-95. PubMed ID: 6060293 [No Abstract] [Full Text] [Related]