Three families with polyneuropathy associated with monoclonal gammopathy

Archives of Neurology

Volumn 57, Issue 5, 2000, Pages 740-742

  Manschot, Sanne M ^a,c   Notermans, Nicolette C ^a   Van Den Berg, Leonard H ^a   Verschuuren, Jan J G M ^b   Lokhorst, Henk M ^d  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^c UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^d NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 1; CHROMOSOME 17; CLINICAL ARTICLE; DEMYELINATING DISEASE; FAMILY STUDY; FEMALE; GENE MUTATION; HUMAN; MALE; MONOCLONAL IMMUNOGLOBULINEMIA; NEUROPHYSIOLOGY; POLYNEUROPATHY; PRIORITY JOURNAL;

EID: 0034082573     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.57.5.740     Document Type: Article

References (12)

1. Latov N. Pathogenesis and therapy of neuropathies associated with monoclonal gammopathies. Ann Neurol. 1995;37(suppl 1):S32-S42.
2. Ropper AH, Gorson KC. Neuropathies associated with paraproteinemia. N Engl J Med. 1998;338:1601-1607.
3. Notermans NC, Wokke JHJ, Lokhorst HM, Franssen H, van den Graaf Y, Jennekens FGI. Polyneuropathy associated with monoclonal gammopathy of undetermined significance: a prospective study of the prognostic value of clinical and laboratory abnormalities. Brain. 1994;117:1385-1393.
4. Bizzaro N, Pasini P. Familial occurrence of multiple myeloma and monoclonal gammopathy of undetermined significance. Haematologica. 1990;75:58-63.
5. Grant JA, Blumenschein GR, Buckley CE. Familial paraproteinemia. Arch Intern Med. 1971;128:427-431.
6. Axelsson U, Hallen J. Familial occurrence of pathological serum proteins of different gamma globulin groups. Lancet. 1965;2:369-370.
7. Youniou P, Le Goff P, Saleun JP, et al. Familial occurrence of monoclonal gammopathies. Biomedicine. 1978;28:226-232
8. Berlin SO, Odenberg H, Weingart L. Familial occurrence of M-components. Acta Med Scand. 1968;183:347-350.
9. Busis NA, Halperin JJ, Stefansson K, et al. Peripheral neuropathy, high serum IgM and paraproteinemia in mother and son. Neurology. 1985;35:679-683
10. Harding AE, Thomas PK. The clinical features of hereditary motor and sensory neuropathy types I and II. Brain. 1980;103:259-280.
11. Saven A, Piro LD. Treatment of hairy cell leukemia. Blood. 1992;79:1111-1120.
12. Horwich MS, Cho L, Parzo RS, Pasner JB. Subacute sensory neuropathy: a remote effect of carcinoma. Ann Neurol. 1977;2:7-19.