BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 38431953)

  • 21. [PNP (purine nucleoside phosphorylase) deficiency].
    Taniguchi A
    Nihon Rinsho; 2003 Jan; 61 Suppl 1():372-6. PubMed ID: 12629750
    [No Abstract]   [Full Text] [Related]  

  • 22. Persistent developmental delay despite successful bone marrow transplantation for purine nucleoside phosphorylase deficiency.
    Baguette C; Vermylen C; Brichard B; Louis J; Dahan K; Vincent MF; Cornu G
    J Pediatr Hematol Oncol; 2002 Jan; 24(1):69-71. PubMed ID: 11902746
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Purine nucleoside phosphorylase].
    Pogosian LG; Akopian ZhI
    Biomed Khim; 2013; 59(5):483-97. PubMed ID: 24479338
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Purine nucleoside phosphorylase deficiency: biochemical properties and heterogeneity in two families.
    Wortmann RL; Andres C; Kaminska J; Mejias E; Gelfand E; Arnold W; Rich K; Fox IH
    Arthritis Rheum; 1979 May; 22(5):524-31. PubMed ID: 36100
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Purine nucleoside phosphorylase deficiency (PNP-def) presenting with lymphopenia and developmental delay: successful correction with umbilical cord blood transplantation.
    Myers LA; Hershfield MS; Neale WT; Escolar M; Kurtzberg J
    J Pediatr; 2004 Nov; 145(5):710-2. PubMed ID: 15520787
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Two novel mutations in a purine nucleoside phosphorylase (PNP)-deficient patient.
    Dalal I; Grunebaum E; Cohen A; Roifman CM
    Clin Genet; 2001 Jun; 59(6):430-7. PubMed ID: 11453975
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Recent advances in understanding and managing adenosine deaminase and purine nucleoside phosphorylase deficiencies.
    Grunebaum E; Cohen A; Roifman CM
    Curr Opin Allergy Clin Immunol; 2013 Dec; 13(6):630-8. PubMed ID: 24113229
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Purine nucleoside phosphorylase (PNP) deficiency].
    Sakiyama T
    Nihon Rinsho; 1996 Dec; 54(12):3328-32. PubMed ID: 8976114
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Upfront Enzyme Replacement via Erythrocyte Transfusions for PNP Deficiency.
    Eichinger A; von Bernuth H; Dedieu C; Schroeder SA; la Marca G; Albert MH; Hauck F
    J Clin Immunol; 2021 Jul; 41(5):1112-1115. PubMed ID: 33641045
    [No Abstract]   [Full Text] [Related]  

  • 30. The First Report of a Pregnancy in a Patient with Purine Nucleoside Phosphorylase Deficiency.
    Martin J; Sharma R; Nelson RP; Schubert F; Weida J
    Fetal Pediatr Pathol; 2016; 35(2):120-3. PubMed ID: 26882246
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Purine nucleoside phosphorylase (PNP) deficiency].
    Sumi S; Wada Y
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):458-9. PubMed ID: 9590100
    [No Abstract]   [Full Text] [Related]  

  • 32. Stroke in purine nucleoside phosphorylase deficiency.
    Tam DA; Leshner RT
    Pediatr Neurol; 1995 Feb; 12(2):146-8. PubMed ID: 7779212
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A novel mutation in purine nucleoside phosphorylase in a child with normal uric acid levels.
    Al-Saud B; Alsmadi O; Al-Muhsen S; Al-Ghonaium A; Al-Dhekri H; Arnaout R; Hershfield MS; Al-Mousa H
    Clin Biochem; 2009 Nov; 42(16-17):1725-7. PubMed ID: 19733163
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cellular immune deficiency with autoimmune hemolytic anemia in purine nucleoside phosphorylase deficiency.
    Rich KC; Arnold WJ; Palella T; Fox IH
    Am J Med; 1979 Jul; 67(1):172-6. PubMed ID: 111549
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Purine Nucleoside Phosphorylase Deficient Severe Combined Immunodeficiencies: A Case Report and Systematic Review (1975-2022).
    Habib Dzulkarnain SM; Hashim IF; Zainudeen ZT; Taib F; Mohamad N; Nasir A; Wan Ab Rahman WS; Ariffin H; Abd Hamid IJ
    J Clin Immunol; 2023 Oct; 43(7):1623-1639. PubMed ID: 37328647
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Direct evidence of autosomal recessive inheritance of Arg24 to termination codon in purine nucleoside phosphorylase gene in a family with a severe combined immunodeficiency patient.
    Sasaki Y; Iseki M; Yamaguchi S; Kurosawa Y; Yamamoto T; Moriwaki Y; Kenri T; Sasaki T; Yamashita R
    Hum Genet; 1998 Jul; 103(1):81-5. PubMed ID: 9737781
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Progressive multifocal leukoencephalopathy in purine nucleoside phosphorylase deficiency.
    Parvaneh N; Ashrafi MR; Yeganeh M; Pouladi N; Sayarifar F; Parvaneh L
    Brain Dev; 2007 Mar; 29(2):124-6. PubMed ID: 16949240
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutations in purine nucleoside phosphorylase deficiency.
    Markert ML; Finkel BD; McLaughlin TM; Watson TJ; Collard HR; McMahon CP; Andrews LG; Barrett MJ; Ward FE
    Hum Mutat; 1997; 9(2):118-21. PubMed ID: 9067751
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Immunodeficiency, Motor Delay, and Hypouricemia Caused by a Novel Mutation of Purine Nucleoside Phosphorylase Gene in an Indian Infant.
    Shah N; Lingappa L; Konanki R; Rani S; Vedam R; Murugan S
    Ann Indian Acad Neurol; 2019; 22(2):231-233. PubMed ID: 31007444
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Therapy in adenosine deaminase and purine nucleoside phosphorylase deficient patients.
    Zegers BJ; Stoop JW
    Clin Biochem; 1983 Feb; 16(1):43-7. PubMed ID: 6407780
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.