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25. [Renal function disorders in congenital metabolic abnormalities. 2. Renal function disorders in Lowe's and de Toni-Fanconi syndrome]. Ito K Nihon Shonika Gakkai Zasshi; 1971 Jun; 75(6):464-75. PubMed ID: 5104633 [No Abstract] [Full Text] [Related]
27. [5-year follow-up of a child with an ophthalmo-cerebro-renal syndrome]. Korniszewski L Pediatr Pol; 1972 Apr; 47(4):481-6. PubMed ID: 5022937 [No Abstract] [Full Text] [Related]
28. [Oculo-cerebro-renal syndrome of Lowe. (Description of a case)]. Berardi G; Brunelli B; Fornaci M; Petrollini R; Piergentili M Minerva Pediatr; 1972 Aug; 24(27):1110-5. PubMed ID: 5084181 [No Abstract] [Full Text] [Related]
30. [Metachromatic leukodystrophy (Scholz-Greenfield disease) associated with Lowe's syndrome with congenital glaucoma without eye enlargement. Clinical, histological and genetic study (literature review concerning these diseases). Ultrastructure of a peripheral nerve and remarks on certain therapeutic possiblities]. Hammami H; Daicker B; Streiff EB; Rabinowicz T; Campiche M; Wiesmann U; Herschkowitz N Bull Mem Soc Fr Ophtalmol; 1973; 86(0):106-27. PubMed ID: 4800102 [No Abstract] [Full Text] [Related]
31. The neuropathology of a peculiar form of cerebro-renal syndrome in a child. Vuia O; Hager H; Rupp H; Koch F Neuropadiatrie; 1973 Jul; 4(3):322-37. PubMed ID: 4800493 [No Abstract] [Full Text] [Related]
32. [Excretion of acid mucopolysaccharides in a child with Lowe's syndrome]. Suschke J; Murken JD Monatsschr Kinderheilkd (1902); 1969 May; 117(5):412-4. PubMed ID: 4256689 [No Abstract] [Full Text] [Related]
33. A possible case of oculo-cerebro-renal (Lowe's) syndrome in a female infant. Lythgoe C; Ramsey MS Can J Ophthalmol; 1973 Oct; 8(4):591-6. PubMed ID: 4751907 [No Abstract] [Full Text] [Related]
34. The ellipsoids (sheaths of Schweigger-Seidal) of the human spleen in various pathological conditions. Dustin P J Pathol; 1971 Jul; 104(3):ii. PubMed ID: 5124993 [No Abstract] [Full Text] [Related]
35. [Anatomo-clinical correlations in some metabolic and tumoral ocular diseases]. Danis MP Bull Soc Ophtalmol Fr; 1973 Feb; 73(2):291-300. PubMed ID: 4794212 [No Abstract] [Full Text] [Related]
36. Lowe's syndrome. Absence of amino acid transport defect in cultured fibroblasts. Bartsocas CS; Erbe RW Acta Paediatr Scand; 1973 Nov; 62(6):615-6. PubMed ID: 4765580 [No Abstract] [Full Text] [Related]
37. [Mental retardation and hereditary enzymopathy (review)]. D'iachkova AIa; Lebedev BV Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1588-93. PubMed ID: 5003148 [No Abstract] [Full Text] [Related]
38. [Lowe's syndrome: multisystemic transport defects]. Robillard JE; Mongeau JG; Morin CL; Dallaire L; Massicotte P Union Med Can; 1973 Jul; 102(7):1496-502. PubMed ID: 4794516 [No Abstract] [Full Text] [Related]
39. [Modern trends in inborn errors of metabolism (reports) (author's transl)]. Bickel H; Molz G Verh Dtsch Ges Pathol; 1971; 55():356-75. PubMed ID: 4130732 [No Abstract] [Full Text] [Related]
40. [Studies on the pathology of oculo-cerebro-renal syndrome (Lowe)]. Arrigoni A; Zunin C Pathologica; 1974; 66(953-954):113-24. PubMed ID: 4418886 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]