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Year Number of Results
2001 3
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Congenital amegakaryocytic thrombocytopenia.
Geddis AE. Geddis AE. Pediatr Blood Cancer. 2011 Aug;57(2):199-203. doi: 10.1002/pbc.22927. Epub 2011 Feb 18. Pediatr Blood Cancer. 2011. PMID: 21337678 Review.
Congenital amegakaryocytic thrombocytopenia (CAMT) is clinically characterized by thrombocytopenia presenting at birth in a child without congenital or skeletal malformations, reduced or absent bone marrow megakaryocytes, and eventual progression to bone marr
Congenital amegakaryocytic thrombocytopenia (CAMT) is clinically characterized by thrombocytopenia presenting at birth
Congenital amegakaryocytic thrombocytopenia - Not a single disease.
Germeshausen M, Ballmaier M. Germeshausen M, et al. Best Pract Res Clin Haematol. 2021 Jun;34(2):101286. doi: 10.1016/j.beha.2021.101286. Epub 2021 Jul 14. Best Pract Res Clin Haematol. 2021. PMID: 34404532 Review.
Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare inherited bone marrow failure syndrome (IBMFS) that is characterized by severe thrombocytopenia at birth due to ineffective megakaryopoiesis and development towards aplastic anemia during the first
Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare inherited bone marrow failure syndrome (IBMFS) that is cha
Congenital amegakaryocytic thrombocytopenia and thrombocytopenia with absent radii.
Geddis AE. Geddis AE. Hematol Oncol Clin North Am. 2009 Apr;23(2):321-31. doi: 10.1016/j.hoc.2009.01.012. Hematol Oncol Clin North Am. 2009. PMID: 19327586 Free PMC article. Review.
Two well-described inherited thrombocytopenia syndromes that present in the newborn period are congenital amegakaryocytic thrombocytopenia (CAMT) and thrombocytopenia with absent radii (TAR). ...
Two well-described inherited thrombocytopenia syndromes that present in the newborn period are congenital amegakaryocytic t
Inherited thrombocytopenia: Congenital amegakaryocytic thrombocytopenia and thrombocytopenia with absent radii.
Geddis AE. Geddis AE. Semin Hematol. 2006 Jul;43(3):196-203. doi: 10.1053/j.seminhematol.2006.04.003. Semin Hematol. 2006. PMID: 16822462 Review.
Thrombocytopenia in the newborn period can signify an inherited platelet disorder. Congenital amegakaryocytic thrombocytopenia (CAMT) and thrombocytopenia with absent radii (TAR) share features of isolated thrombocytopenia, reduced or absent marrow megakaryoc …
Thrombocytopenia in the newborn period can signify an inherited platelet disorder. Congenital amegakaryocytic thrombocytope
Congenital amegakaryocytic thrombocytopenia: clinical presentation, diagnosis, and treatment.
Ballmaier M, Germeshausen M. Ballmaier M, et al. Semin Thromb Hemost. 2011 Sep;37(6):673-81. doi: 10.1055/s-0031-1291377. Epub 2011 Nov 18. Semin Thromb Hemost. 2011. PMID: 22102270 Review.
Congenital amegakaryocytic thrombocytopenia (CAMT, MIM #604498) is a rare inherited bone marrow failure syndrome presenting as isolated hypomegakaryocytic thrombocytopenia at birth without other characteristic physical anomalies. ...
Congenital amegakaryocytic thrombocytopenia (CAMT, MIM #604498) is a rare inherited bone marrow failure syndrome presen
Advances in the understanding of congenital amegakaryocytic thrombocytopenia.
Ballmaier M, Germeshausen M. Ballmaier M, et al. Br J Haematol. 2009 Jun;146(1):3-16. doi: 10.1111/j.1365-2141.2009.07706.x. Epub 2009 Apr 21. Br J Haematol. 2009. PMID: 19388932 Free article. Review.
Congenital amegakaryocytic thrombocytopenia (MIM #604498) is an extremely rare inherited bone marrow failure syndrome, usually presenting as a severe thrombocytopenia at birth due to ineffective megakaryocytopoiesis and no characteristic physical anomalies. .
Congenital amegakaryocytic thrombocytopenia (MIM #604498) is an extremely rare inherited bone marrow failure syndrome,
Changes in megakaryopoiesis over ontogeny and their implications in health and disease.
Davenport P, Liu ZJ, Sola-Visner M. Davenport P, et al. Platelets. 2020 Aug 17;31(6):692-699. doi: 10.1080/09537104.2020.1742879. Epub 2020 Mar 21. Platelets. 2020. PMID: 32200697 Free PMC article. Review.
We will also discuss the implications of these findings on the ways MKs interact with the environment, the response of neonates to thrombocytopenia, the pathogenesis of Down syndrome-transient myeloproliferative disorder (TMD), and the developmental stage specific-manifestations …
We will also discuss the implications of these findings on the ways MKs interact with the environment, the response of neonates to thrombocy …
CRISPR/Cas9-mediated gene editing. A promising strategy in hematological disorders.
Ugalde L, Fañanas S, Torres R, Quintana-Bustamante O, Río P. Ugalde L, et al. Cytotherapy. 2023 Mar;25(3):277-285. doi: 10.1016/j.jcyt.2022.11.014. Epub 2023 Jan 5. Cytotherapy. 2023. PMID: 36610813 Review.
This technology has been applied in different congenital blood disorders, such as primary immunodeficiencies, X-linked severe combined immunodeficiency, X-linked chronic granulomatous disease or Wiskott-Aldrich syndrome, and inherited bone marrow failure syndromes, such as Fancon …
This technology has been applied in different congenital blood disorders, such as primary immunodeficiencies, X-linked severe combined immun …
28 results