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PUBMED FOR HANDHELDS

Journal Abstract Search


96 related items for PubMed ID: 3292862

  • 21. [An unusual form of the Muckle and Wells syndrome: perception deafness, hypogonadism, repeated febrile urticaria and arthritis, with renal insufficiency].
    Fabre J, Mach RS, Perrottet C.
    Minerva Nefrol; 1973; 20(4):276-9. PubMed ID: 4789746
    [No Abstract] [Full Text] [Related]

  • 22. Amyloidosis, deafness, urticaria, and limb pains: a hereditary syndrome.
    Black JT.
    Ann Intern Med; 1969 May; 70(5):989-94. PubMed ID: 5769632
    [No Abstract] [Full Text] [Related]

  • 23. Muckle-Wells syndrome: clinical and histological skin findings compatible with cold air urticaria in a large kindred.
    Haas N, Küster W, Zuberbier T, Henz BM.
    Br J Dermatol; 2004 Jul; 151(1):99-104. PubMed ID: 15270877
    [Abstract] [Full Text] [Related]

  • 24. [Periodic disease and the Muckle-Wells syndrome].
    Mamou H, Mamou JE, de Regnault DM.
    Nouv Presse Med; 1974 May 25; 3(21):1363-4. PubMed ID: 4849369
    [No Abstract] [Full Text] [Related]

  • 25. Urticaria, arthralgia, and nephropathy without amyloidosis: another variant of the Muckle-Wells syndrome?
    Throssell D, Feehally J, Trembath R, Walls J.
    Clin Genet; 1996 Mar 25; 49(3):130-3. PubMed ID: 8737977
    [Abstract] [Full Text] [Related]

  • 26. Deafness, urticaria and amyloidosis: a sporadic case with a chromosomal aberration.
    Andersen V, Buch NH, Jensen MK, Killmann SA.
    Am J Med; 1967 Mar 25; 42(3):449-56. PubMed ID: 6018861
    [No Abstract] [Full Text] [Related]

  • 27. Recovery from deafness in a patient with Muckle-Wells syndrome treated with anakinra.
    Mirault T, Launay D, Cuisset L, Hachulla E, Lambert M, Queyrel V, Quemeneur T, Morell-Dubois S, Hatron PY.
    Arthritis Rheum; 2006 May 25; 54(5):1697-700. PubMed ID: 16646042
    [Abstract] [Full Text] [Related]

  • 28. Muckle-Wells syndrome: report of six cases with hyperpigmented sclerodermoid skin lesions.
    El-Darouti MA, Marzouk SA, Abdel-Halim MR.
    Int J Dermatol; 2006 Mar 25; 45(3):239-44. PubMed ID: 16533222
    [Abstract] [Full Text] [Related]

  • 29. [Progressive craal nerve neuropathy with dystrophy of the cornea--a new heritable amyloidosis syndrome].
    Meretoja J.
    Duodecim; 1970 Mar 25; 86(1):34-41. PubMed ID: 4192479
    [No Abstract] [Full Text] [Related]

  • 30. [Successful treatment of clinical manifestations of Muckle-Wells syndrome with anakinra].
    Dybowski F, Jakobs B, Altmeyer P, Braun J.
    Dtsch Med Wochenschr; 2006 Aug 25; 131(34-35):1863-6. PubMed ID: 16915547
    [Abstract] [Full Text] [Related]

  • 31. Identification of a locus on chromosome 1q44 for familial cold urticaria.
    Hoffman HM, Wright FA, Broide DH, Wanderer AA, Kolodner RD.
    Am J Hum Genet; 2000 May 25; 66(5):1693-8. PubMed ID: 10741953
    [Abstract] [Full Text] [Related]

  • 32. [Muckle-Wells syndrome. Apropos of a case].
    Milán JA, Palma A.
    Med Clin (Barc); 1989 Feb 18; 92(6):239. PubMed ID: 2709915
    [No Abstract] [Full Text] [Related]

  • 33. Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44.
    Cuisset L, Drenth JP, Berthelot JM, Meyrier A, Vaudour G, Watts RA, Scott DG, Nicholls A, Pavek S, Vasseur C, Beckmann JS, Delpech M, Grateau G.
    Am J Hum Genet; 1999 Oct 18; 65(4):1054-9. PubMed ID: 10486324
    [Abstract] [Full Text] [Related]

  • 34. The Muckle-Wells syndrome and the major histocompatibility complex.
    Hedon V, Kaplan C, Vaudour G, Muller JY.
    Tissue Antigens; 1983 Apr 18; 21(4):318-9. PubMed ID: 6857626
    [No Abstract] [Full Text] [Related]

  • 35. A probable case of Muckle-Wells syndrome.
    Kagami S, Saeki H, Kuwano Y, Imakado S, Tamaki K.
    J Dermatol; 2006 Feb 18; 33(2):118-21. PubMed ID: 16556280
    [Abstract] [Full Text] [Related]

  • 36. Hereditary deafness in man.
    Konigsmark BW.
    N Engl J Med; 1969 Oct 09; 281(15):827-32 concl. PubMed ID: 4309240
    [No Abstract] [Full Text] [Related]

  • 37. [Improvement of Muckle-Wells syndrome by hemodialysis].
    Cledes J, Herve JP, Bernard E, Treguer H.
    Nouv Presse Med; 1969 Oct 09; 9(30):2076-7. PubMed ID: 7402926
    [No Abstract] [Full Text] [Related]

  • 38. [Ocular lesions in primary familial amyloidosis (a syndrome associating opacitieis of the vitreous body, vascular lesions of the retina and an amyloid neuropathy)].
    Franceschetti AT, Rabinowicz T.
    J Genet Hum; 1969 Oct 09; 17(3):349-66. PubMed ID: 4319009
    [No Abstract] [Full Text] [Related]

  • 39. [Histopathological study of familial systemic amyloidosis with latticed corneal dystrophy].
    Wang SJ.
    Zhonghua Yi Xue Za Zhi; 1985 Feb 09; 65(2):78-9. PubMed ID: 3921213
    [No Abstract] [Full Text] [Related]

  • 40. An autosomal dominant periodic fever associated with AA amyloidosis in a north Indian family maps to distal chromosome 1q.
    McDermott MF, Aganna E, Hitman GA, Ogunkolade BW, Booth DR, Hawkins PN.
    Arthritis Rheum; 2000 Sep 09; 43(9):2034-40. PubMed ID: 11014353
    [Abstract] [Full Text] [Related]


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