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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

164 related items for PubMed ID: 24619057

  • 41. Secondary hypogammaglobulinemia in Waldmann's disease treated with subcutaneous immunoglobulins.
    Patuzzo G, Tinazzi E, Micheletti M, Puccetti A, Lunardi C.
    Eur Ann Allergy Clin Immunol; 2016 Mar; 48(2):55-7. PubMed ID: 26934740
    [Abstract] [Full Text] [Related]

  • 42. Disorders of the intestinal mesenteric lymphatic system.
    Fox U, Lucani G.
    Lymphology; 1993 Jun; 26(2):61-6. PubMed ID: 8355519
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  • 45. The importance and function of footwear in managing lymphoedema.
    Farrelly I.
    Br J Community Nurs; 2008 Oct; 13(10):S10-4. PubMed ID: 19057476
    [Abstract] [Full Text] [Related]

  • 46. Severe lymphedema, intestinal lymphangiectasia, seizures and mild mental retardation: further case of Hennekam syndrome with a severe phenotype.
    Forzano F, Faravelli F, Loy A, Di Rocco M.
    Am J Med Genet; 2002 Jul 22; 111(1):68-70. PubMed ID: 12124738
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  • 47. A case report of Hennekam syndrome with a mutation in the CCBE1 gene.
    Durak T, Karaer D, Karaer K.
    Clin Dysmorphol; 2024 Apr 01; 33(2):87-89. PubMed ID: 38441203
    [No Abstract] [Full Text] [Related]

  • 48. Are you handling genital oedema confidently?
    Noble-Jones R, Thomas MJ, Davies L, Morgan K.
    Br J Community Nurs; 2019 Oct 01; 24(Sup10):S19-S22. PubMed ID: 31604039
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  • 49. Primary lymphedema: clinical features and management in 138 pediatric patients.
    Schook CC, Mulliken JB, Fishman SJ, Grant FD, Zurakowski D, Greene AK.
    Plast Reconstr Surg; 2011 Jun 01; 127(6):2419-2431. PubMed ID: 21617474
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  • 51. [Variant analysis of CCBE1 gene in a case of Hennekam lymphangiectasia-lymphedema syndrome type 1].
    Ren Y, Liu Y, Lyu Y, Gao M, Wang D, Wan Y, Ma J, Shen N, Gai Z.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jun 10; 37(6):669-672. PubMed ID: 32472549
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  • 52. Lymphoedema: pathophysiology and classification.
    Browse NL, Stewart G.
    J Cardiovasc Surg (Torino); 1985 Jun 10; 26(2):91-106. PubMed ID: 3884629
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  • 54. Management of lymphoedema.
    Yüksel A, Gürbüz O, Velioğlu Y, Kumtepe G, Şenol S.
    Vasa; 2016 Jun 10; 45(4):283-91. PubMed ID: 27428496
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  • 55. Expansion of the phenotype in Hennekam syndrome: a case with new manifestations.
    Angle B, Hersh JH.
    Am J Med Genet; 1997 Aug 08; 71(2):211-4. PubMed ID: 9217224
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  • 57. Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24.
    Brice G, Mansour S, Bell R, Collin JR, Child AH, Brady AF, Sarfarazi M, Burnand KG, Jeffery S, Mortimer P, Murday VA.
    J Med Genet; 2002 Jul 08; 39(7):478-83. PubMed ID: 12114478
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  • 58. Classification of lymphatic-system malformations in primary lymphoedema based on MR lymphangiography.
    Liu NF, Yan ZX, Wu XF.
    Eur J Vasc Endovasc Surg; 2012 Sep 08; 44(3):345-9. PubMed ID: 22831870
    [Abstract] [Full Text] [Related]

  • 59. Patient experience: raising a child with primary lymphoedema.
    Illsley's J.
    Br J Nurs; 2018 Jun 28; 27(12):678-680. PubMed ID: 29953273
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