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Journal Abstract Search

105 related items for PubMed ID: 8822580

  • 41.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 42. The genomic architecture of the PROS1 gene underlying large tandem duplication mutation that causes thrombophilia from hereditary protein S deficiency.
    Seo JY, Lee KO, Kim SH, Oh D, Kim DK, Kim HJ.
    Gene; 2014 Sep 01; 547(2):295-9. PubMed ID: 24992033
    [Abstract] [Full Text] [Related]

  • 43. A novel nonsense mutation Tyr301* of PROS1 causing protein S deficiency.
    Jang MA, Kim SH, Kim DK, Kim HJ.
    Blood Coagul Fibrinolysis; 2015 Mar 01; 26(2):223-4. PubMed ID: 25255242
    [Abstract] [Full Text] [Related]

  • 44. Homozygosity for the protein S Heerlen allele is associated with type I PS deficiency in a thrombophilic pedigree with multiple risk factors.
    Espinosa-Parrilla Y, Navarro G, Morell M, Abella E, Estivill X, Sala N.
    Thromb Haemost; 2000 Jan 01; 83(1):102-6. PubMed ID: 10669162
    [Abstract] [Full Text] [Related]

  • 45. Single nucleotide polymorphisms and haplotypes of protein C and protein S genes in the Thai population.
    Chumpia W, Peerapittayamongkol C, Angchaisuksiri P, Komanasin N, Muta K, Kuaha K, Iida H, Inoue S, Wada Y, Kurihara M, Hamasaki N, Fucharoen S.
    Blood Coagul Fibrinolysis; 2006 Jan 01; 17(1):13-8. PubMed ID: 16607073
    [Abstract] [Full Text] [Related]

  • 46. [Molecular anomalies of coagulation inhibitors].
    Aiach M.
    Nouv Rev Fr Hematol (1978); 1993 Jun 01; 35(3):265-6. PubMed ID: 8337141
    [No Abstract] [Full Text] [Related]

  • 47. Protein S deficiency.
    D'Angelo A, Viganò D'Angelo S.
    Haematologica; 2008 Apr 01; 93(4):498-501. PubMed ID: 18379009
    [No Abstract] [Full Text] [Related]

  • 48.
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    [No Abstract] [Full Text] [Related]

  • 49. Hereditary protein S deficiency from a novel large deletion mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification (MLPA).
    Yoo JH, Kim HJ, Maeng HY, Kim YA, Sun YK, Song JW, Choi JR, Kim SH, Lee KA.
    Thromb Res; 2009 Mar 01; 123(5):793-5. PubMed ID: 19168201
    [No Abstract] [Full Text] [Related]

  • 50. [Type I hereditary protein C deficiency due to C5498T mutation in protein C gene].
    Zhou RF, Wang HL, Fu QH, Wang WB, Wu WM, Ding QL, Xie S, Hu YQ, Wang XF, Wang ZY.
    Zhonghua Yi Xue Za Zhi; 2003 Oct 10; 83(19):1694-7. PubMed ID: 14642106
    [Abstract] [Full Text] [Related]

  • 51. [Primary thalamic hemorrhage penetrating to the lateral ventricle in an infant with abnormal protein S(protein S-Tokushima)].
    Inoha S, Inamura T, Nakamizo A, Amano T, Hamasaki N, Mizuno Y, Nishio H, Fukui M.
    No To Shinkei; 2001 Apr 10; 53(4):377-80. PubMed ID: 11360479
    [Abstract] [Full Text] [Related]

  • 52. [PROSI Mutation With Clinical Heterogeneity in Protein S Deficiency:Report of One Case].
    Wei XY, Wang J, Tan BY, Li ZJ.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2023 Oct 10; 45(5):863-866. PubMed ID: 37621108
    [Abstract] [Full Text] [Related]

  • 53.
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  • 54.
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  • 55. Identification of 19 protein S gene mutations in patients with phenotypic protein S deficiency and thrombosis. Protein S Study Group.
    Simmonds RE, Ireland H, Kunz G, Lane DA.
    Blood; 1996 Dec 01; 88(11):4195-204. PubMed ID: 8943854
    [Abstract] [Full Text] [Related]

  • 56. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 01; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 57. Identification of two different mutations causing protein S deficiency in two unrelated Belgian families using a nonisotopic scanning and sequencing method.
    Messiaen L, Callens T, Baele G.
    Haemostasis; 1997 Aug 01; 27(5):228-36. PubMed ID: 9690481
    [Abstract] [Full Text] [Related]

  • 58. [Blood coagulation disorders--special reference to thrombosis].
    Saito H.
    Nihon Naika Gakkai Zasshi; 1999 Sep 10; 88(9):1670-8. PubMed ID: 10581745
    [No Abstract] [Full Text] [Related]

  • 59. A frequent mutation in the protein S gene results in cryptic splicing.
    Mustafa S, Pabinger I, Mannhalter C.
    Br J Haematol; 1997 Jun 10; 97(3):555-7. PubMed ID: 9207399
    [Abstract] [Full Text] [Related]

  • 60.
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