Literature DB >> 3153315

Alport's syndrome or hereditary nephritis?

F A Flinter1, M Bobrow, C Chantler.   

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Year:  1987        PMID: 3153315     DOI: 10.1007/bf00849251

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


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  15 in total

1.  Hereditary chronic kidney disease: an alternative to partial sex-linkage in the Utah kindred.

Authors:  J B GRAHAM
Journal:  Am J Hum Genet       Date:  1959-12       Impact factor: 11.025

2.  A heredo-familial syndrome characterized by renal disease, inner ear deafness, and ocular changes.

Authors:  E SOHAR
Journal:  Harefuah       Date:  1954-10-15

3.  Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus.

Authors:  G S Spear; R J Slusser
Journal:  Am J Pathol       Date:  1972-11       Impact factor: 4.307

4.  Pathologic characteristics of hereditary nephritis.

Authors:  J Churg; R L Sherman
Journal:  Arch Pathol       Date:  1973-06

5.  Alport's syndrome. A report of 58 cases and a review of the literature.

Authors:  M Gubler; M Levy; M Broyer; C Naizot; G Gonzales; D Perrin; R Habib
Journal:  Am J Med       Date:  1981-03       Impact factor: 4.965

6.  Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome).

Authors:  N Hinglais; J P Grünfeld; E Bois
Journal:  Lab Invest       Date:  1972-11       Impact factor: 5.662

7.  Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes?

Authors:  J A Govan
Journal:  Br J Ophthalmol       Date:  1983-08       Impact factor: 4.638

8.  Early pathologic features of hereditary nephritis: a clinicopathologic correlation.

Authors:  W M O'Neill; R P Mennemeyer; H A Bloomer; C L Atkin
Journal:  Pathol Res Pract       Date:  1980       Impact factor: 3.250

Review 9.  Variants of Alport's syndrome.

Authors:  J P Grünfeld; G Grateau; L H Noel; R Charbonneau; M C Gubler; C O Savage; C M Lockwood
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

10.  Genetic heterogeneity among kindreds with Alport syndrome.

Authors:  S J Hasstedt; C L Atkin; A C San Juan
Journal:  Am J Hum Genet       Date:  1986-06       Impact factor: 11.025

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  8 in total

Review 1.  The investigation of haematuria.

Authors:  R H White
Journal:  Arch Dis Child       Date:  1989-01       Impact factor: 3.791

2.  Mutation in the alpha 5(IV) collagen chain in juvenile-onset Alport syndrome without hearing loss or ocular lesions: detection by denaturing gradient gel electrophoresis of a PCR product.

Authors:  J Zhou; J M Hertz; K Tryggvason
Journal:  Am J Hum Genet       Date:  1992-06       Impact factor: 11.025

Review 3.  Alport's syndrome.

Authors:  F Flinter
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

4.  A new syndrome of autosomal recessive nephropathy, deafness, and hyperparathyroidism.

Authors:  B D Edwards; M A Patton; S A Dilly; J B Eastwood
Journal:  J Med Genet       Date:  1989-05       Impact factor: 6.318

Review 5.  The application of molecular biology to the prenatal diagnosis of renal disease.

Authors:  F A Flinter; M Bobrow
Journal:  Pediatr Nephrol       Date:  1988-07       Impact factor: 3.714

6.  Alport's syndrome and hereditary motor and sensory neuropathy type I--an unfortunate coincidence.

Authors:  J E Deal; S M Hall; R A Hughes; S P Rigden
Journal:  Pediatr Nephrol       Date:  1993-04       Impact factor: 3.714

7.  The Alport nephropathy: clinicopathological correlations.

Authors:  Richard H R White; Faro Raafat; David V Milford; Filadelfia Komianou; Nadeem E Moghal
Journal:  Pediatr Nephrol       Date:  2005-04-26       Impact factor: 3.714

8.  The development of anti-glomerular basement membrane nephritis in two children with Alport's syndrome after renal transplantation: characterization of the antibody target.

Authors:  L P vd Heuvel; C H Schröder; C O Savage; D Menzel; K J Assmann; L A Monnens; J H Veerkamp
Journal:  Pediatr Nephrol       Date:  1989-10       Impact factor: 3.714

  8 in total

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