Two Cases of Aminoaciduria, Ocular Changes and Retarded Mental and Somatic Development (Lowe's Syndrome)
- 1 September 1960
- journal article
- case report
- Published by Wiley in Acta Paediatrica
- Vol. 49 (5) , 635-644
- https://doi.org/10.1111/j.1651-2227.1960.tb07781.x
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- Amino aciduria, congenital defects, and mental retardation: A preliminary reportThe Journal of Pediatrics, 1956
- Hyperamino-aciduria in Lignac-Fanconi Disease, in Galactosaemia and in an Obscure SyndromeArchives of Disease in Childhood, 1954
- THE VARIOUS ETIOLOGIES MET IN THE UNITED STATES WITH EMPHASIS ON THAT RESULTING FROM A SPECIFIC FORM OF RENAL ACIDOSIS, THE THERAPEUTIC INDICATIONS FOR EACH ETIOLOGICAL SUB-GROUP, AND THE RELATIONSHIP BETWEEN OSTEOMALACIA AND MILKMANʼS SYNDROMEMedicine, 1946
- THE RENAL EXCRETION OF INORGANIC PHOSPHATE IN RELATION TO THE ACTION OF VITAMIN D AND PARATHYROID HORMONE 1Journal of Clinical Investigation, 1941
- A COMPARISON OF THE EFFECTS OF VITAMIN D, DIHYDRO-TACHYSTEROL (A.T. 10), AND PARATHYROID EXTRACT ON THE DISORDERED METABOLISM OF RICKETSJournal of Clinical Investigation, 1939