Skip to main content

. 1967 Nov 11;97(20):1193–1198.

Charcot-Marie-Tooth disease and nephritis.

G Lemieux, J A Neemeh

PMCID: PMC1923627 PMID: 6054293

1193

Images in this article

Fig. 1
on p.1194

Fig. 3a
on p.1195

Fig. 3b
on p.1195

Fig. 4
on p.1196

Fig. 5
on p.1196

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

ASBURY A. K., VICTOR M., ADAMS R. D. Uremic polyneuropathy. Arch Neurol. 1963 Apr;8:413–428. doi: 10.1001/archneur.1963.00460040083008. [DOI] [PubMed] [Google Scholar]
COHEN M. M., CASSADY G., HANNA B. L. A genetic study of hereditary renal dysfunction with associated nerve deafness. Am J Hum Genet. 1961 Dec;13:379–389. [PMC free article] [PubMed] [Google Scholar]
DAWSON C. W., ROBERTS J. B. CHARCOT-MARIE-TOOTH DISEASE. JAMA. 1964 May 18;188:659–661. doi: 10.1001/jama.1964.03060330039010. [DOI] [PubMed] [Google Scholar]
Dubach U. C., Minder F. C., Antener I. Familial nephropathy and deafness: first observation of a family and close relatives in Switzerland. Helv Med Acta. 1966 Apr;33(1):36–43. [PubMed] [Google Scholar]
GOLDBLOOM R. B., FRASER F. C., WAUGH D., ARONOVITCH M., WIGLESWORTH F. W. Hereditary renal disease associated with nerve deafness and ocular lesions. Pediatrics. 1957 Aug;20(2):241–252. [PubMed] [Google Scholar]
LUCAS G. J., FORSTER F. M. Charcot-Marie-Tooth disease with associated myopathy. A report of a family. Neurology. 1962 Sep;12:629–636. doi: 10.1212/wnl.12.9.629. [DOI] [PubMed] [Google Scholar]
MAHOUDEAU D., DAUM S., LEMPERIERE Un cas de maladie de Friedreich avec amyotrophie du type Charcot-Marie; étude clinique. Rev Neurol (Paris) 1950 Oct;83(4):281–284. [PubMed] [Google Scholar]
MARIN O. S., TYLER H. R. Hereditary interstitial nephritis associated with polyneuropathy. Neurology. 1961 Nov;11:999–1005. doi: 10.1212/wnl.11.11.999. [DOI] [PubMed] [Google Scholar]
OHLSSON L. CONGENITAL RENAL DISEASE, DEAFNESS AND MYOPIA IN ONE FAMILY. Acta Med Scand. 1963 Jul;174:77–84. doi: 10.1111/j.0954-6820.1963.tb07893.x. [DOI] [PubMed] [Google Scholar]
PERKOFF G. T., STEPHENS F. E., DOLOWITZ D. A., TYLER F. H. A clinical study of hereditary interstitial pyelonephritis. AMA Arch Intern Med. 1951 Aug;88(2):191–200. doi: 10.1001/archinte.1951.03810080059006. [DOI] [PubMed] [Google Scholar]
Perkoff G. T. The hereditary renal diseases. N Engl J Med. 1967 Jul 13;277(2):79–contd. doi: 10.1056/NEJM196707132770206. [DOI] [PubMed] [Google Scholar]
SERRATRICE G., TATOSSIAN A., POINSO Y. AMYOTROPHIE DE CHARCOT-MARIE ASSOCI'EE 'A UNE ATROPHIE OPTIQUE BILAT'ERALE. Presse Med. 1964 Oct 17;72:2535–2536. [PubMed] [Google Scholar]
SMITH C. K. Vertebral deformities and other anomalies in Charcot-Marie-Tooth disease. Neurology. 1958 Jun;8(6):481–486. doi: 10.1212/wnl.8.6.481. [DOI] [PubMed] [Google Scholar]
SOHAR E. Renal disease, inner ear deafness, and ocular changes; a new heredofamilial syndrome. AMA Arch Intern Med. 1956 May;97(5):627–630. doi: 10.1001/archinte.1956.00250230121013. [DOI] [PubMed] [Google Scholar]
TENCKHOFF H. A., BOEN S. T., JEBSEN R. H., SPIEGLER J. H. POLYNEUROPATHY IN CHRONIC RENAL INSUFFICIENCY. JAMA. 1965 Jun 28;192:1121–1124. doi: 10.1001/jama.1965.03080260009003. [DOI] [PubMed] [Google Scholar]
WALLACE I. R., JONES J. H. Familial glomerulonephritis and aminoaciduria. Lancet. 1960 Apr 30;1(7131):941–944. doi: 10.1016/s0140-6736(60)90834-5. [DOI] [PubMed] [Google Scholar]
WHALEN R. E., HUANG S., PESCHEL E., McINTOSH H. D. Hereditary nephropathy, deafness and renal foam cells. Am J Med. 1961 Aug;31:171–186. doi: 10.1016/0002-9343(61)90107-3. [DOI] [PubMed] [Google Scholar]
WILLIAMSON D. A. Alport's syndrome of hereditary nephritis with deafness. Lancet. 1961 Dec 16;2(7216):1321–1323. doi: 10.1016/s0140-6736(61)90899-6. [DOI] [PubMed] [Google Scholar]
van Buchem F. S., Beetstra A. Hereditary renal disease associated with deafness--Alport's syndrome. Acta Med Scand. 1966 Mar;179(3):319–328. doi: 10.1111/j.0954-6820.1966.tb05464.x. [DOI] [PubMed] [Google Scholar]

ACTIONS

PDF (2.0 MB)

RESOURCES