Literature DB >> 6054293

Charcot-Marie-Tooth disease and nephritis.

G Lemieux, J A Neemeh.   

Abstract

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Year:  1967        PMID： 6054293      PMCID： PMC1923627     

Source DB:  PubMed          Journal:  Can Med Assoc J        ISSN： 0008-4409            Impact factor:   8.262


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  19 in total

1.  POLYNEUROPATHY IN CHRONIC RENAL INSUFFICIENCY.

Authors:  H A TENCKHOFF; S T BOEN; R H JEBSEN; J H SPIEGLER
Journal:  JAMA       Date:  1965-06-28       Impact factor: 56.272

2.  Uremic polyneuropathy.

Authors:  A K ASBURY; M VICTOR; R D ADAMS
Journal:  Arch Neurol       Date:  1963-04

3.  Familial glomerulonephritis and aminoaciduria.

Authors:  I R WALLACE; J H JONES
Journal:  Lancet       Date:  1960-04-30       Impact factor: 79.321

4.  Renal disease, inner ear deafness, and ocular changes; a new heredofamilial syndrome.

Authors:  E SOHAR
Journal:  AMA Arch Intern Med       Date:  1956-05

5.  Hereditary interstitial nephritis associated with polyneuropathy.

Authors:  O S MARIN; H R TYLER
Journal:  Neurology       Date:  1961-11       Impact factor: 9.910

6.  Charcot-Marie-Tooth disease with associated myopathy. A report of a family.

Authors:  G J LUCAS; F M FORSTER
Journal:  Neurology       Date:  1962-09       Impact factor: 9.910

7.  A clinical study of hereditary interstitial pyelonephritis.

Authors:  G T PERKOFF; F E STEPHENS; D A DOLOWITZ; F H TYLER
Journal:  AMA Arch Intern Med       Date:  1951-08

8.  Hereditary renal disease associated with deafness--Alport's syndrome.

Authors:  F S van Buchem; A Beetstra
Journal:  Acta Med Scand       Date:  1966-03

9.  Familial nephropathy and deafness: first observation of a family and close relatives in Switzerland.

Authors:  U C Dubach; F C Minder; I Antener
Journal:  Helv Med Acta       Date:  1966-04

10.  Alport's syndrome of hereditary nephritis with deafness.

Authors:  D A WILLIAMSON
Journal:  Lancet       Date:  1961-12-16       Impact factor: 79.321
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  7 in total

1.  Familial spastic paraplegia, bilateral sensorineural deafness, and intellectual retardation associated with a progressive nephropathy.

Authors:  J S Fitzsimmons; A R Watson; D Mellor; P R Guilbert
Journal:  J Med Genet       Date:  1988-03       Impact factor: 6.318

Review 2.  Hereditary Podocytopathies in Adults: The Next Generation.

Authors:  Olivia Boyer; Guillaume Dorval; Aude Servais
Journal:  Kidney Dis (Basel)       Date:  2017-05-31

3.  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

4.  Novel INF2 mutation p. L77P in a family with glomerulopathy and Charcot-Marie-Tooth neuropathy.

Authors:  Patricia Q Rodriguez; Bernhard Lohkamp; Gianni Celsi; Christoph Johannes Mache; Michaela Auer-Grumbach; Annika Wernerson; Nobuyuki Hamajima; Karl Tryggvason; Jaakko Patrakka
Journal:  Pediatr Nephrol       Date:  2012-09-11       Impact factor: 3.714

5.  Hereditary nephropathy with hematuria (Alport's syndrome).

Authors:  A Chiricosta; S L Jindal; J Metuzals; B Koch
Journal:  Can Med Assoc J       Date:  1970-02-28       Impact factor: 8.262

Review 6.  Formins in Human Disease.

Authors:  Leticia Labat-de-Hoz; Miguel A Alonso
Journal:  Cells       Date:  2021-09-27       Impact factor: 6.600

7.  Membranous Nephropathy in a Patient with Charcot-Marie-Tooth Disease: Association of Myelin Mutations.

Authors:  U Anandh; R Nikalji; A Parick
Journal:  Indian J Nephrol       Date:  2018 Sep-Oct
  7 in total

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