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Can Med Assoc J. 1962 July 7; 87(1): 1–4.1.
PMCID: PMC1849299

The Familial Occurrence of Erythromelalgia and Nephritis

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Selected References

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  • HAWKINS CF, SMITH OE. Renal dysplasia in a family with multiple hereditary abnormalities including iliac horns. Lancet. 1950 Apr 29;1(6609):803–808. [PubMed]
  • PERKOFF GT, STEPHENS FE, DOLOWITZ DA, TYLER FH. A clinical study of hereditary interstitial pyelonephritis. AMA Arch Intern Med. 1951 Aug;88(2):191–200. [PubMed]
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  • HILSON D. Malformation of ears as sign of malformation of genito-urinary tract. Br Med J. 1957 Oct 5;2(5048):785–789. [PMC free article] [PubMed]
  • PERKOFF GT, NUGENT CA, Jr, DOLOWITZ DA, STEPHENS FE, CARNES WH, TYLER FH. A follow-up study of hereditary chronic nephritis. AMA Arch Intern Med. 1958 Nov;102(5):733–746. [PubMed]
  • KLOTZ RE. Congenital hereditary kidney disease and hearing loss: a case history. AMA Arch Otolaryngol. 1959 May;69(5):560–562. [PubMed]
  • LOUGHRIDGE LW. Renal abnormalities in the Marfan syndrome. Q J Med. 1959 Oct;28:531–544. [PubMed]
  • WALLACE IR, JONES JH. Familial glomerulonephritis and aminoaciduria. Lancet. 1960 Apr 30;1(7131):941–944. [PubMed]
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  • FREEDMAN P, PETERS JH, KARK RM. Localization of gamma-globulin in the diseased kidney. Arch Intern Med. 1960 Apr;105:524–535. [PubMed]
  • CAMPBELL A, CONWAY H. The Rose Bradford kidney. Familial occurrence. Scott Med J. 1961 Apr;6:153–155. [PubMed]
  • WHALEN RE, HUANG S, PESCHEL E, McINTOSH HD. Hereditary nephropathy, deafness and renal foam cells. Am J Med. 1961 Aug;31:171–186. [PubMed]

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