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Journal Abstract Search

91 related items for PubMed ID: 4789746

  • 21. The 'Muckle-Wells' syndrome.
    Muckle TJ.
    Br J Dermatol; 1979 Jan; 100(1):87-92. PubMed ID: 427013
    [No Abstract] [Full Text] [Related]

  • 22. Intrafamilial variable phenotypic expression of a CIAS1 mutation: from Muckle-Wells to chronic infantile neurological cutaneous and articular syndrome.
    Hentgen V, Despert V, Leprêtre AC, Cuisset L, Chevrant-Breton J, Jégo P, Chalès G, Gall EL, Delpech M, Grateau G.
    J Rheumatol; 2005 Apr; 32(4):747-51. PubMed ID: 15801036
    [Abstract] [Full Text] [Related]

  • 23. The arthropathy of the Muckle-Wells syndrome.
    Watts RA, Nicholls A, Scott DG.
    Br J Rheumatol; 1994 Dec; 33(12):1184-7. PubMed ID: 8000753
    [Abstract] [Full Text] [Related]

  • 24. [Improvement of Muckle-Wells syndrome by hemodialysis].
    Cledes J, Herve JP, Bernard E, Treguer H.
    Nouv Presse Med; 1994 Dec; 9(30):2076-7. PubMed ID: 7402926
    [No Abstract] [Full Text] [Related]

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

  • 26. 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; 54(5):1697-700. PubMed ID: 16646042
    [Abstract] [Full Text] [Related]

  • 27. [Muckle-Wells syndrome associated with idiopathic interstitial pneumopathy].
    Gómez Rodríguez F, Muñoz Lucena F, Peña Griñán N, Umbria Domínguez S.
    An Med Interna; 1991 Feb; 8(2):85-6. PubMed ID: 1893010
    [Abstract] [Full Text] [Related]

  • 28. Juberg-Marsidi syndrome: report of an additional case.
    Tsukahara M, Nasu T, Takihara H, Hattori Y, Nakane H, Kamata K, Mitsui H, Hayashida S.
    Am J Med Genet; 1995 Sep 25; 58(4):353-5. PubMed ID: 8533845
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. [Muckle-Wells syndrome (urticaria, hearing loss and amyloidosis)].
    Krámer M, Somlai B.
    Orv Hetil; 1982 Jan 24; 123(4):221-2. PubMed ID: 7063241
    [No Abstract] [Full Text] [Related]

  • 31. [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]

  • 32. Alstrom syndrome.
    Garg RA, Singh J, Mathur BB.
    Indian Pediatr; 1991 Jul 18; 28(7):799-801. PubMed ID: 1800358
    [No Abstract] [Full Text] [Related]

  • 33. 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 18; 49(3):130-3. PubMed ID: 8737977
    [Abstract] [Full Text] [Related]

  • 34. Waardenburg-like features with cataracts, small head size, joint abnormalities, hypogonadism, and osteosarcoma.
    Parry DM, Safyer AW, Mulvihill JJ.
    J Med Genet; 1978 Feb 18; 15(1):66-9. PubMed ID: 273099
    [Abstract] [Full Text] [Related]

  • 35. Urticaria, deafness, and amyloidosis: a new heredo-familial syndrome.
    MUCKLE TJ, WELLSM.
    Q J Med; 1962 Apr 18; 31():235-48. PubMed ID: 14476827
    [No Abstract] [Full Text] [Related]

  • 36. [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]

  • 37. Diagnosis of Muckle-Wells syndrome - 33 years later.
    Fye KH, Siegel DH, Connolly MK.
    J Rheumatol; 2007 Dec 25; 34(12):2505-6. PubMed ID: 18061973
    [No Abstract] [Full Text] [Related]

  • 38. Amyloidosis, deafness, urticaria, and limb pains: a hereditary syndrome.
    Black JT.
    Ann Intern Med; 1969 May 25; 70(5):989-94. PubMed ID: 5769632
    [No Abstract] [Full Text] [Related]

  • 39. Branchio-oto-renal syndrome.
    Garg A, Wadhera R, Gulati SP, Kumar A.
    J Assoc Physicians India; 2008 Nov 25; 56():904-5. PubMed ID: 19263692
    [Abstract] [Full Text] [Related]

  • 40. Diffuse polymicrogyria associated with an unusual pattern of multiple congenital anomalies including turribrachycephaly and hypogenitalism.
    Cohn RD, Gillessen-Kaesbach G, Dobyns WB, Kahn T, Lenard HG, Voit T.
    Am J Med Genet; 1996 May 03; 63(1):314-7. PubMed ID: 8723127
    [Abstract] [Full Text] [Related]

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