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Journal Abstract Search

134 related items for PubMed ID: 25521170

  • 21. Silvery-gray hair in a newborn.
    Wong L, Yano S.
    JAMA; 2012 Aug 08; 308(6):617-8. PubMed ID: 22871872
    [No Abstract] [Full Text] [Related]

  • 22. [A 28-year-old man with hepatosplenomegaly and fever].
    Muntañola A, Rodríguez S, Giné E.
    Med Clin (Barc); 2014 Sep 15; 143(6):261-7. PubMed ID: 24856173
    [No Abstract] [Full Text] [Related]

  • 23. Anakinra as an agent to control hemophagocytic lymphohistiocytosis in Griscelli type 2.
    Kim SR, Kissoon-Larkin T, Horn B, Elder M.
    Pediatr Blood Cancer; 2019 Dec 15; 66(12):e27997. PubMed ID: 31535456
    [No Abstract] [Full Text] [Related]

  • 24. [A hemophagocytic syndrome revealing a Griscelli syndrome type 2].
    Jennane S, El Kababri M, Hessissen L, Kili A, Nachef MN, Messaoudi N, Doghmi K, Mikdame M, El Khorassani M, Khattab M.
    Ann Biol Clin (Paris); 2013 Dec 15; 71(4):461-4. PubMed ID: 23906575
    [Abstract] [Full Text] [Related]

  • 25. Griscelli syndrome: a case report.
    Mehdizadeh M, Zamani G.
    Pediatr Hematol Oncol; 2007 Dec 15; 24(7):525-9. PubMed ID: 17786788
    [Abstract] [Full Text] [Related]

  • 26. Accelerated phase in partial albinism with immunodeficiency (Griscelli syndrome): genetics and stem cell transplantation in a 2-month-old girl.
    Baumeister FA, Stachel D, Schuster F, Schmid I, Schaller M, Wolff H, Weiss M, Belohradsky BH.
    Eur J Pediatr; 2000 Dec 15; 159(1-2):74-8. PubMed ID: 10653334
    [Abstract] [Full Text] [Related]

  • 27. [The Griscelli-Prunieras syndrome: a case report].
    Salazar-Cabrera AN, Matos-Martínez M, Sánchez-Villegas MC, Lázaro-Castillo LM, Méndez-León J, Martínez-Amigon J, Aguilar M, García-Escobar B.
    Bol Med Hosp Infant Mex; 1993 Jul 15; 50(7):503-7. PubMed ID: 8363750
    [Abstract] [Full Text] [Related]

  • 28. Griscelli syndrome.
    Malhotra AK, Bhaskar G, Nanda M, Kabra M, Singh MK, Ramam M.
    J Am Acad Dermatol; 2006 Aug 15; 55(2):337-40. PubMed ID: 16844525
    [Abstract] [Full Text] [Related]

  • 29. A RAB27A duplication in several cases of Griscelli syndrome type 2: An explanation for cases lacking a genetic diagnosis.
    Grandin V, Sepulveda FE, Lambert N, Al Zahrani M, Al Idrissi E, Al-Mousa H, Almanjomi F, Al-Ghonaium A, K Habazi M, A Alghamdi H, Picard C, Bole-Feysot C, Nitschke P, Ménasché G, de Saint Basile G.
    Hum Mutat; 2017 Oct 15; 38(10):1355-1359. PubMed ID: 28585352
    [Abstract] [Full Text] [Related]

  • 30. A teenage boy with late onset hemophagocytic lymphohistiocytosis with predominant neurologic disease and perforin deficiency.
    Beaty AD, Weller C, Levy B, Vogler C, Ferguson WS, Bicknese A, Knutsen AP.
    Pediatr Blood Cancer; 2008 May 15; 50(5):1070-2. PubMed ID: 18074390
    [Abstract] [Full Text] [Related]

  • 31. Molecular analysis and clinical findings of Griscelli syndrome patients.
    Durmaz A, Ozkinay F, Onay H, Tombuloglu M, Atay A, Gursel O, Peker E, Atmaca M, Genel F, Bozabali S, Akin H, Ozkinay C.
    J Pediatr Hematol Oncol; 2012 Oct 15; 34(7):541-4. PubMed ID: 22983416
    [Abstract] [Full Text] [Related]

  • 32. Dyserythropoiesis due to reactive hemophagocytic lymphohistiocytosis.
    Xu Z, Van der Jagt R.
    Blood; 2016 Oct 27; 128(17):2190. PubMed ID: 27789440
    [No Abstract] [Full Text] [Related]

  • 33. Plasmodium vivax malaria-associated hemophagocytic lymphohistiocytosis in a young man with pancytopenia and fever.
    Bae E, Jang S, Park CJ, Chi HS.
    Ann Hematol; 2011 Apr 27; 90(4):491-2. PubMed ID: 20721557
    [No Abstract] [Full Text] [Related]

  • 34. PARTIAL OCULOCUTANEOUS ALBINISM AND IMMUNODEFICIENCY SYNDROMES: TEN YEARS EXPERIENCE FROM A SINGLE CENTER IN TURKEY.
    Patiroglu T, Akar HH, Unal E, Chiang SC, Schlums H, Tesi B, Ozkars MY, Karakukcu M.
    Genet Couns; 2016 Apr 27; 27(1):67-76. PubMed ID: 27192893
    [Abstract] [Full Text] [Related]

  • 35. Fever, Splenomegaly, and Pancytopenia: Histoplasma-Associated Hemophagocytic Lymphohistiocytosis.
    Gupta A, Agrawal M, Jaso J.
    J Gen Intern Med; 2017 Sep 27; 32(9):1060-1062. PubMed ID: 28299604
    [No Abstract] [Full Text] [Related]

  • 36. Hemophagocytic lymphohistiocytosis in a neonate with cutis marmorata telangiectatica congenita.
    Elahi B, Ramyar A.
    Saudi Med J; 2006 Nov 27; 27(11):1751-3. PubMed ID: 17106557
    [Abstract] [Full Text] [Related]

  • 37. Griscelli syndrome associated with hemophagocytic lymphohistiocytosis.
    Love PB, Patterson SS, Prose NS, Atwater AR.
    J Drugs Dermatol; 2012 Sep 27; 11(9):1126. PubMed ID: 23135662
    [No Abstract] [Full Text] [Related]

  • 38. Hair pigment distribution changes after haematopoietic stem cell transplantation in Griscelli syndrome type 2.
    Yamazaki-Nakashimada MA, Roldán-Marín R, Toussaint-Caire S, Olaya-Vargas A, Ramírez-Uribe N, Rivas-Larrauri F, Durán-McKinster C, Alcántara-Ortigoza MA, González-Del Angel A, Orozco-Covarrubias L, Scheffler-Mendoza S, Saez-de-Ocariz M.
    J Eur Acad Dermatol Venereol; 2021 Jan 27; 35(1):e53-e56. PubMed ID: 32594618
    [No Abstract] [Full Text] [Related]

  • 39. Cutaneous granulomas as the presenting manifestation of Griscelli syndrome type 2.
    Gotesman R, Ramien M, Armour CM, Pham-Huy A, Kirshen C.
    Pediatr Dermatol; 2021 Jan 27; 38(1):194-197. PubMed ID: 32965739
    [Abstract] [Full Text] [Related]

  • 40. Severe hemorrhagic coagulopathy with hemophagocytic lymphohistiocytosis secondary to Epstein-Barr virus-associated T-cell lymphoproliferative disorder.
    Nawathe PA, Ravindranath TM, Satwani P, Baird JS.
    Pediatr Crit Care Med; 2013 May 27; 14(4):e176-81. PubMed ID: 23439459
    [Abstract] [Full Text] [Related]

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