These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

100 related articles for article (PubMed ID: 30575022)

  • 61. Heterozygous Missense Variant in EIF6 gene: a novel form of Shwachman-Diamond Syndrome?
    Koh AL; Bonnard C; Binte Ali NA; Reversade B; Jamuar S
    Am J Med Genet A; 2022 Jan; 188(1):384. PubMed ID: 34528395
    [No Abstract]   [Full Text] [Related]  

  • 62. Author Correction: Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors.
    Hamabata T; Umeda K; Kouzuki K; Tanaka T; Daifu T; Nodomi S; Saida S; Kato I; Baba S; Hiramatsu H; Osawa M; Niwa A; Saito MK; Kamikubo Y; Adachi S; Hashii Y; Shimada A; Watanabe H; Osafune K; Okita K; Nakahata T; Watanabe K; Takita J; Heike T
    Sci Rep; 2021 Jan; 11(1):2107. PubMed ID: 33462257
    [No Abstract]   [Full Text] [Related]  

  • 63. Oh rats! Intracellular rod-like inclusions in an adolescent with Shwachman-Diamond syndrome.
    Mayhew J; Luttrell H; Barros K; Blazin L; Nichols C; Avashia-Khemka N; Lavik JP; Relich RF; Skinner D; Zhou J; Saraf A; Khaitan A
    Pediatr Blood Cancer; 2024 May; 71(5):e30918. PubMed ID: 38391125
    [No Abstract]   [Full Text] [Related]  

  • 64. From Challenge to Opportunity: How Shwachman-Diamond Syndrome Became a Promising Target for Therapy Development.
    Hars ES; McReynolds LJ
    Clin Pharmacol Ther; 2024 Jul; ():. PubMed ID: 39039619
    [No Abstract]   [Full Text] [Related]  

  • 65. Hepatic phenotypes of EFL1-related Shwachman-Diamond syndrome in a biopsy-validated study.
    Zhu B; Guo Y; Lv S; Ling X; You S
    J Hepatol; 2024 Sep; 81(3):e102-e104. PubMed ID: 38703831
    [No Abstract]   [Full Text] [Related]  

  • 66. Expression of Concern: Shwachman-Diamond Syndrome in a Child Presenting With Chronic Diarrhea: A Rare Case in Family Medicine Practice.
    Alshammari M; Aljohani MA; Hashash JM; Alsaedi HA; Alobaidi WY; Alhuzali NK; Alnumani MS; Alrashidi AH; Al-Battniji SA; Alotaibi NA; Alhumaidi NK; Alajaimi AN; Alqurashi RS; Albishri AT; Alshammari KH
    Cureus; 2022 Apr; 14(4):x15. PubMed ID: 35463585
    [No Abstract]   [Full Text] [Related]  

  • 67. 2018 Harry Shwachman Award.
    Di Lorenzo C
    J Pediatr Gastroenterol Nutr; 2019 Mar; 68(3):291. PubMed ID: 30614955
    [No Abstract]   [Full Text] [Related]  

  • 68. Clinical features and outcomes of patients with Shwachman-Diamond syndrome and myelodysplastic syndrome or acute myeloid leukaemia: a multicentre, retrospective, cohort study.
    Myers KC; Furutani E; Weller E; Siegele B; Galvin A; Arsenault V; Alter BP; Boulad F; Bueso-Ramos C; Burroughs L; Castillo P; Connelly J; Davies SM; DiNardo CD; Hanif I; Ho RH; Karras N; Manalang M; McReynolds LJ; Nakano TA; Nalepa G; Norkin M; Oberley MJ; Orgel E; Pastore YD; Rosenthal J; Walkovich K; Larson J; Malsch M; Elghetany MT; Fleming MD; Shimamura A
    Lancet Haematol; 2020 Mar; 7(3):e238-e246. PubMed ID: 31879230
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Potentials of ribosomopathy gene as pharmaceutical targets for cancer treatment.
    Wang M; Vulcano S; Xu C; Xie R; Peng W; Wang J; Liu Q; Jia L; Li Z; Li Y
    J Pharm Anal; 2024 Mar; 14(3):308-320. PubMed ID: 38618250
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Shwachman-Diamond syndrome: implications for understanding the molecular basis of leukaemia.
    Dror Y
    Expert Rev Mol Med; 2008 Dec; 10():e38. PubMed ID: 19102804
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Shwachman-Diamond syndrome.
    Dror Y
    Pediatr Blood Cancer; 2005 Dec; 45(7):892-901. PubMed ID: 16047374
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Genetics for understanding the clinical features of Shwachman-Diamond Syndrome.
    Nacci L
    Br J Haematol; 2019 Mar; 184(5):710-711. PubMed ID: 30575022
    [No Abstract]   [Full Text] [Related]  

  • 73. Shwachman-Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability.
    Valli R; Minelli A; Galbiati M; D'Amico G; Frattini A; Montalbano G; Khan AW; Porta G; Millefanti G; Olivieri C; Cipolli M; Cesaro S; Pasquali F; Danesino C; Cazzaniga G; Maserati E
    Br J Haematol; 2019 Mar; 184(6):974-981. PubMed ID: 30585299
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman-Diamond-like syndrome.
    Saettini F; Cattoni A; D'Angio' M; Corti P; Maitz S; Pagni F; Seminati D; Pezzoli L; Iascone M; Biondi A; Bonanomi S
    Br J Haematol; 2020 May; 189(4):e171-e174. PubMed ID: 32196641
    [No Abstract]   [Full Text] [Related]  

  • 75. Autosomal dominant Shwachman-Diamond syndrome with a novel heterozygous missense variant in the SRP54 gene causing severe phenotypic features.
    McCarthy P; Cotter M; Smith OP
    Br J Haematol; 2022 Feb; 196(3):e39-e42. PubMed ID: 34549814
    [No Abstract]   [Full Text] [Related]  

  • 76. A novel Drosophila model for neurodevelopmental disorders associated with Shwachman-Diamond syndrome.
    Takai A; Chiyonobu T; Ueoka I; Tanaka R; Tozawa T; Yoshida H; Morimoto M; Hosoi H; Yamaguchi M
    Neurosci Lett; 2020 Nov; 739():135449. PubMed ID: 33115644
    [TBL] [Abstract][Full Text] [Related]  

  • 77.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 78.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 79.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 80.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.