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Results: 1 to 20 of 27

Related Articles by Review for PubMed (Select 14246065)

1.

THE OCULO-CEREBRO-RENAL SYNDROME OF LOWE.

RICHARDS W, DONNELL GN, WILSON WA, STOWENS D, PERRY T.

Am J Dis Child. 1965 Mar;109:185-203. No abstract available.

PMID:
14246065
2.

Oculo-cerebro-renal syndrome. A review.

Abbassi V, Lowe CU, Calcagno PL.

Am J Dis Child. 1968 Feb;115(2):145-68. Review. No abstract available.

PMID:
4865974
3.

Urinary screening tests in the infant and young child.

Bradley GM.

Hum Pathol. 1971 Jun;2(2):309-20. Review. No abstract available.

PMID:
4256386
4.

Urinary screening tests in the infant and young child.

Bradley GM.

Med Clin North Am. 1971 Nov;55(6):1457-71. Review. No abstract available.

PMID:
4256889
5.

[Mental retardation and hereditary enzymopathy (review)].

D'iachkova AIa, Lebedev BV.

Zh Nevropatol Psikhiatr Im S S Korsakova. 1971;71(10):1588-93. Review. Russian. No abstract available.

PMID:
5003148
6.

[RENAL TUBULAR DISEASES, WITH SPECIAL REFERENCE TO AMINOACIDURIA].

MILNE MD.

Recenti Prog Med. 1964 Mar;36:163-86. Review. Italian. No abstract available.

PMID:
14153013
7.

RENAL ACIDOSIS AND RENAL EXCRETION OF ACID IN HEALTH AND DISEASE.

RELMAN AS.

Adv Intern Med. 1964;12:295-347. Review. No abstract available.

PMID:
14268281
8.

[ON THE PATHOPHYSIOLOGY AND CLINICAL MANIFESTATIONS OF DISORDERS OF RENAL TUBULAR PARTIAL FUNCTION].

GEROK W, PABST K.

Munch Med Wochenschr. 1965 Jan 8;107:73-82. Review. German. No abstract available.

PMID:
14301178
9.

THE PRIMARY AMINO-ACIDOPATHIES. GENETIC DEFECTS IN THE METABOLISM OF THE AMINO ACIDS.

DIGEORGE AM, AUERBACH VH.

Pediatr Clin North Am. 1963 Aug;10:723-44. Review. No abstract available.

PMID:
14145016
10.

[The urinary excretion of amino acids in endogenous oligophrenia].

Constantinidis J.

Schweiz Arch Neurol Neurochir Psychiatr. 1965;96(1):1-49. Review. French. No abstract available.

PMID:
5320184
11.

RENAL TUBULAR DISORDERS.

MILNE MD, LOUGHRIDGE LW.

Dis Mon. 1964 Oct;89:SUPPL 1964:1+. Review. No abstract available.

PMID:
14214262
12.

[CITRULLINURIA].

FREYCON F, FREYCON MT.

Pediatrie. 1963;18:847-9. Review. French. No abstract available.

PMID:
14106631
13.

How to measure proteinuria?

McIntyre NJ, Taal MW.

Curr Opin Nephrol Hypertens. 2008 Nov;17(6):600-3. doi: 10.1097/MNH.0b013e328313675c. Review.

PMID:
18941353
14.

Congenital cataract, microphthalmia, hypoplasia of corpus callosum and hypogenitalism: report and review of Micro syndrome.

Derbent M, Agras PI, Gedik S, Oto S, Alehan F, Saatçi U.

Am J Med Genet A. 2004 Jul 30;128A(3):232-4. Review.

PMID:
15216542
15.
16.

HYPERKALEMIA AND HYPOKALEMIA.

PAPPER S, WHANG R.

Dis Mon. 1964 Jun;128:1964:1-29. Review. No abstract available.

PMID:
14156889
17.

[Renal function and pregnancy].

De Martino A, Bausano G.

Recenti Prog Med. 1983 Jun;74(6):755-8. Review. Italian. No abstract available.

PMID:
6351204
18.

Osteoporosis in children with neuromuscular diseases and inborn errors of metabolism.

Plotkin H, Sueiro R.

Minerva Pediatr. 2007 Apr;59(2):129-35. Review.

PMID:
17404563
19.

Uric acid changes in urine and plasma: an effective tool in screening for purine inborn errors of metabolism and other pathological conditions.

Simoni RE, Gomes LN, Scalco FB, Oliveira CP, Aquino Neto FR, de Oliveira ML.

J Inherit Metab Dis. 2007 Jun;30(3):295-309. Epub 2007 May 19. Review.

PMID:
17520339
20.

[CONGENITAL ERRORS OF METABOLISM].

FREZAL J.

Ann Genet. 1964;7:37-43. Review. French. No abstract available.

PMID:
14242106
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