176 related articles for article (PubMed ID: 388203)
1. Hereditary tubular disorders.
Woolf LI
Monogr Pathol; 1979; 20():218-38. PubMed ID: 388203
[No Abstract] [Full Text] [Related]
2. Inherited tubule disorders.
DeFronzo RA; Thier SO
Hosp Pract (Off Ed); 1982 Feb; 17(2):111-7, 121-8. PubMed ID: 6281157
[No Abstract] [Full Text] [Related]
3. Genetics of renal transport disorders.
Segal S
Prog Clin Biol Res; 1989; 305():101-9. PubMed ID: 2668967
[No Abstract] [Full Text] [Related]
4. Clinical phenotypes in kidney transport disorders.
Bartsocas CS; Crawford JD
Birth Defects Orig Artic Ser; 1974; 10(4):118-26. PubMed ID: 4377865
[TBL] [Abstract][Full Text] [Related]
5. [Genetic bases of metabolic tubular nephropathies].
Savi M
Minerva Med; 1979 Oct; 70(44):3001-13. PubMed ID: 386171
[No Abstract] [Full Text] [Related]
6. Hereditary tubular disorders of the Fanconi type and the idiopathic Fanconi syndrome.
Bickel H; Manz F
Prog Clin Biol Res; 1989; 305():111-35. PubMed ID: 2668968
[No Abstract] [Full Text] [Related]
7. [Primary and secondary hyperaminoaciduria in children (review of the literature)].
Lebedev VP; Iur'eva EA; Mukhina IuG; Buravina TA; Koroleva IA
Vopr Okhr Materin Det; 1970 Nov; 15(11):64-8. PubMed ID: 4928437
[No Abstract] [Full Text] [Related]
8. The prognosis and management of renal tubular disorders.
Milne MD
Proc R Soc Med; 1967 Nov; 60(11 Part 1):1149-52. PubMed ID: 6060714
[No Abstract] [Full Text] [Related]
9. Disorders of renal amino acid transport.
Segal S
N Engl J Med; 1976 May; 294(19):1044-51. PubMed ID: 943698
[No Abstract] [Full Text] [Related]
10. Aminoaciduria and hyperaminoaciduria in childhood.
Brodehl J; Bickel H
Clin Nephrol; 1973; 1(3):149-68. PubMed ID: 4593448
[No Abstract] [Full Text] [Related]
11. Hypophosphataemic osteomalacia and Fanconi syndrome of adult onset with dominant inheritance. Possible relationship with diabetes mellitus.
Smith R; Lindenbaum RH; Walton RJ
Q J Med; 1976 Jul; 45(179):387-400. PubMed ID: 948541
[TBL] [Abstract][Full Text] [Related]
12. [Disorders of renal tubular transport of amino acids, hexose and phosphate].
Hasegawa H; Takayanagi K; Mitarai T
Nihon Rinsho; 2006 Feb; 64 Suppl 2():522-7. PubMed ID: 16523947
[No Abstract] [Full Text] [Related]
13. Hereditary metabolic bone diseases.
Harrison HE; Harrison HC
Clin Orthop Relat Res; 1964; 33():147-63. PubMed ID: 5889018
[No Abstract] [Full Text] [Related]
14. Linkage analyses in families with nephrogenic diabetes insipidus.
Knoers NV; van der Heyden H; van Oost BA; Monnens L; Willems J; Ropers HH
Prog Clin Biol Res; 1989; 305():149-55. PubMed ID: 2569742
[No Abstract] [Full Text] [Related]
15. Renal phenotype in Lowe Syndrome: a selective proximal tubular dysfunction.
Bockenhauer D; Bokenkamp A; van't Hoff W; Levtchenko E; Kist-van Holthe JE; Tasic V; Ludwig M
Clin J Am Soc Nephrol; 2008 Sep; 3(5):1430-6. PubMed ID: 18480301
[TBL] [Abstract][Full Text] [Related]
16. Pathology of aminoacidurias. II. Visceral lesions.
Roels H
Monogr Hum Genet; 1972; 6():79-98. PubMed ID: 4663917
[No Abstract] [Full Text] [Related]
17. [Renal tubular diseases].
Sergeeva TV
Med Sestra; 1978 May; 37(5):28-32. PubMed ID: 207945
[No Abstract] [Full Text] [Related]
18. [CYSTINOSIS WITH AMINO-PHOSPHATE DIABETES WITHOUT GLYCOSURIA IN A 26-MONTH-OLD GIRL. DIAGNOSIS BY RENAL BIOPSY].
FONTAN A; VERGER P; BENTEGEAT J; KERMAREC J; BATTIN JJ; CHANNAROND J
Arch Fr Pediatr; 1963; 20():793-802. PubMed ID: 14049367
[No Abstract] [Full Text] [Related]
19. [ON THE PATHOPHYSIOLOGY AND CLINICAL MANIFESTATIONS OF DISORDERS OF RENAL TUBULAR PARTIAL FUNCTION].
GEROK W; PABST K
Munch Med Wochenschr; 1965 Jan; 107():73-82. PubMed ID: 14301178
[No Abstract] [Full Text] [Related]
20. [On some aspects of renal tubule physiopathology in childhood].
Bottone E; Macchia PA; Baldini G; Bani E
Minerva Pediatr; 1973 Jul; 25(25):1073-118. PubMed ID: 4356737
[No Abstract] [Full Text] [Related]
[Next] [New Search]
