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Results: 15

Related Articles by Review for PubMed (Select 2339699)

1.

Molecular cloning of alpha 5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locus.

Myers JC, Jones TA, Pohjolainen ER, Kadri AS, Goddard AD, Sheer D, Solomon E, Pihlajaniemi T.

Am J Hum Genet. 1990 Jun;46(6):1024-33.

2.

Molecular genetics of Alport syndrome.

Tryggvason K, Zhou J, Hostikka SL, Shows TB.

Kidney Int. 1993 Jan;43(1):38-44. Review.

PMID:
8433568
3.

Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes.

Kashtan CE.

Medicine (Baltimore). 1999 Sep;78(5):338-60. Review.

PMID:
10499074
4.

Alport syndrome, basement membranes and collagen.

Kashtan CE, Kleppel MM, Butkowski RJ, Michael AF, Fish AJ.

Pediatr Nephrol. 1990 Sep;4(5):523-32. Review.

PMID:
2242324
5.

Alport syndrome: from bedside to genome to bedside.

Kashtan CE, Michael AF.

Am J Kidney Dis. 1993 Nov;22(5):627-40. Review.

PMID:
8238007
6.

Alport syndrome. A review of the ocular manifestations.

Colville DJ, Savige J.

Ophthalmic Genet. 1997 Dec;18(4):161-73. Review.

PMID:
9457747
7.

Clinical and molecular diagnosis of Alport syndrome.

Kashtan CE.

Proc Assoc Am Physicians. 1995 Oct;107(3):306-13. Review.

PMID:
8608415
8.

[Molecular genetics of Alport syndrome].

Yamazaki H, Saito A, Nakagawa Y, Arakawa M.

Nihon Rinsho. 1992 Dec;50(12):3021-6. Review. Japanese.

PMID:
1491454
9.

Organization and expression of basement membrane collagen IV genes and their roles in human disorders.

Sado Y, Kagawa M, Naito I, Ueki Y, Seki T, Momota R, Oohashi T, Ninomiya Y.

J Biochem. 1998 May;123(5):767-76. Review.

10.

Alport syndrome and diffuse leiomyomatosis. Clinical aspects, pathology, molecular biology and extracellular matrix studies. A synthesis.

Garcia-Torres R, Cruz D, Orozco L, Heidet L, Gubler MC.

Nephrologie. 2000;21(1):9-12. Review.

PMID:
10730274
11.

The clinical spectrum of type IV collagen mutations.

Lemmink HH, Schröder CH, Monnens LA, Smeets HJ.

Hum Mutat. 1997;9(6):477-99. Review.

PMID:
9195222
12.

Pathology of glomerular basement membrane nephropathy.

Hudson BG, Kalluri R, Tryggvason K.

Curr Opin Nephrol Hypertens. 1994 May;3(3):334-9. Review.

PMID:
7922261
13.

The gene for X-linked Kallmann syndrome: a human neuronal migration defect.

Ballabio A, Camerino G.

Curr Opin Genet Dev. 1992 Jun;2(3):417-21. Review.

PMID:
1504616
14.

Cloning of Alport syndrome gene.

Tryggvason K.

Ann Med. 1991 Aug;23(3):237-9. Review. No abstract available.

PMID:
1930913
15.

[Gene analysis and kidney diseases].

Ishida M.

Nihon Naika Gakkai Zasshi. 1993 Mar 10;82(3):463-8. Review. Japanese. No abstract available.

PMID:
8391051
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