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Journal Abstract Search


123 related items for PubMed ID: 15861202

  • 21. Prenatal panel screening considerations for non-neuronopathic Gaucher disease in the Ashkenazi-Jewish population.
    Kannai R, Chertok IR.
    Isr Med Assoc J; 2006 May; 8(5):347-50. PubMed ID: 16805236
    [Abstract] [Full Text] [Related]

  • 22. [Gaucher disease type 1, incidentally found on a periodic physical examination].
    Yoshida K, Kawai N, Matsuda A, Murohashi I, Jinnai I, Ino H, Bessho M, Takeuchi H, Saitoh M, Hirashima K.
    Rinsho Ketsueki; 1996 Jan; 37(1):82-5. PubMed ID: 8683874
    [Abstract] [Full Text] [Related]

  • 23. Molecular characterization of type 3 (neuronopathic) Gaucher disease in Thai patients.
    Suwannarat P, Keeratichamroen S, Wattanasirichaigoon D, Ngiwsara L, Cairns JR, Svasti J, Visudtibhan A, Pangkanon S.
    Blood Cells Mol Dis; 2007 Jan; 39(3):348-52. PubMed ID: 17689991
    [Abstract] [Full Text] [Related]

  • 24. [A 32-year old male patient with pathological humeral fracture, splenomegaly and thrombocytopenia].
    Dürr EM, Geiss HC, Pontz BF, Parhofer KG.
    Internist (Berl); 2004 Apr; 45(4):455-60. PubMed ID: 15151139
    [Abstract] [Full Text] [Related]

  • 25. [Neonatal cholestasis in an intermediate phenotype of type 2 Gaucher disease].
    Ben Turkia H, Tebib N, Kasdallah N, Abdelmoula MS, Azzouz H, Ben Chehida A, Caillaud C, Ben Dridi MF.
    Arch Pediatr; 2009 Mar; 16(3):255-7. PubMed ID: 19181499
    [No Abstract] [Full Text] [Related]

  • 26. Fetal and neonatal hepatic tumors.
    Isaacs H.
    J Pediatr Surg; 2007 Nov; 42(11):1797-803. PubMed ID: 18022426
    [Abstract] [Full Text] [Related]

  • 27. The clinical course of untreated Gaucher disease in 22 patients over 10 years: hematological and skeletal manifestations.
    Piran S, Roberts A, Patterson MA, Amato D.
    Blood Cells Mol Dis; 2009 Nov; 43(3):289-93. PubMed ID: 19793665
    [Abstract] [Full Text] [Related]

  • 28. Thrombocytopenia and GBA gene mutation in a patient with adult type 1 Gaucher disease.
    Wan L, Wu H, Xie F, Nie Y.
    Platelets; 2017 Dec; 28(8):829-831. PubMed ID: 28580830
    [Abstract] [Full Text] [Related]

  • 29. Long-term follow-up of a patient with neonatal form of Gaucher disease.
    Gragnaniello V, Cazzorla C, Gueraldi D, Loro C, Massa P, Puma A, Cananzi M, Salviati L, Burlina AP, Burlina AB.
    Am J Med Genet A; 2023 Jul; 191(7):1917-1922. PubMed ID: 37009750
    [Abstract] [Full Text] [Related]

  • 30. Disease state awareness in Gaucher disease: a Q&A expert roundtable discussion.
    Mistry PK, Weinthal JA, Weinreb NJ.
    Clin Adv Hematol Oncol; 2012 Jun; 10(6 Suppl 8):1-16. PubMed ID: 22895100
    [Abstract] [Full Text] [Related]

  • 31. Divergent phenotypes in Gaucher disease implicate the role of modifiers.
    Goker-Alpan O, Hruska KS, Orvisky E, Kishnani PS, Stubblefield BK, Schiffmann R, Sidransky E.
    J Med Genet; 2005 Jun; 42(6):e37. PubMed ID: 15937077
    [Abstract] [Full Text] [Related]

  • 32. Maternal hypertension and neonatal outcome among small for gestational age infants.
    Bageris A, Cohen T.
    Obstet Gynecol; 2005 Dec; 106(6):1416; author reply 1416-7. PubMed ID: 16319274
    [No Abstract] [Full Text] [Related]

  • 33. Gaucher disease among Chinese patients: review on genotype/phenotype correlation from 29 patients and identification of novel and rare alleles.
    Choy FY, Zhang W, Shi HP, Zay A, Campbell T, Tang N, Ferreira P.
    Blood Cells Mol Dis; 2007 Dec; 38(3):287-93. PubMed ID: 17196853
    [Abstract] [Full Text] [Related]

  • 34. Impact of cesarean section on neonatal mortality rates among very preterm infants in the United States, 2000-2003.
    Malloy MH.
    Pediatrics; 2008 Aug; 122(2):285-92. PubMed ID: 18676545
    [Abstract] [Full Text] [Related]

  • 35. Maternal thrombocytopenia-absent radius syndrome complicated by severe pre-eclampsia.
    Wax JR, Crabtree C, Blackstone J, Pinette MG, Cartin A.
    J Matern Fetal Neonatal Med; 2009 Feb; 22(2):175-7. PubMed ID: 19253167
    [Abstract] [Full Text] [Related]

  • 36. [Biochemical and molecular diagnosis of Gaucher disease in Tunisia].
    Dandana A, Ferchichi S, Khedhiri S, Chkioua L, Jaidane Z, Monastiri K, Ben Khelifa S, Ben Mansour R, Maire I, Froissart R, Bonnet V, Laradi S, Miled A.
    Ann Biol Clin (Paris); 2007 Feb; 65(6):647-52. PubMed ID: 18039610
    [Abstract] [Full Text] [Related]

  • 37. Anti-HPA-9bw (Maxa) fetomaternal alloimmunization, a clinically severe neonatal thrombocytopenia: difficulties in diagnosis and therapy and report on eight families.
    Kaplan C, Porcelijn L, Vanlieferinghen P, Julien E, Bianchi F, Martageix C, Bertrand G, Jallu V.
    Transfusion; 2005 Nov; 45(11):1799-803. PubMed ID: 16271107
    [Abstract] [Full Text] [Related]

  • 38. [Gaucher's disease uncovered late].
    Ben Said F, Mseddi S, Ben Aribia N, Elloumi M, Ben Jemaa M, Ben Amar M, Boudawara T, Kallel C, Makni F, Souissi T.
    Tunis Med; 2004 May; 82(5):453-6. PubMed ID: 15453048
    [Abstract] [Full Text] [Related]

  • 39. Pediatric non-neuronopathic Gaucher disease: presentation, diagnosis and assessment. Consensus statements.
    Grabowski GA, Andria G, Baldellou A, Campbell PE, Charrow J, Cohen IJ, Harris CM, Kaplan P, Mengel E, Pocovi M, Vellodi A.
    Eur J Pediatr; 2004 Feb; 163(2):58-66. PubMed ID: 14677061
    [Abstract] [Full Text] [Related]

  • 40. Randomized prospective comparative study of ursodeoxycholic acid and S-adenosyl-L-methionine in the treatment of intrahepatic cholestasis of pregnancy.
    Binder T, Salaj P, Zima T, Vítek L.
    J Perinat Med; 2006 Feb; 34(5):383-91. PubMed ID: 16965225
    [Abstract] [Full Text] [Related]


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