Výsledky vyhledávání - "Anthony Macheta"

The diagnostic conundrum posed by Hypereosinophilia with a foot drop: A Case Report

Autor: Fiona Wood, Natassja Moriarty, Anthony Macheta, Jonathan Moriarty

Publikováno v: International Journal of Case Reports. :136

We present a case of an 81-year-old asthmatic female with a left foot drop and an incidental finding of hypereosinophilia with an initial differential diagnosis of Eosinophilic Granulomatosis with Polyangiitis (EGPA). However, after extensive investi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2d32f2c28aab305e5df7102d815abc11
https://doi.org/10.28933/ijcr-2020-05-2105

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Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy

Autor: Jude Fitzgibbon, Brian Leber, Gary D. Sinclair, Anna Koochin, T. Andrew Lister, Clayton A. Smith, Jane Stevens, John A. Liu Yin, Anthony Macheta, Peter R. E. Johnson, Carolyn Owen, Shannon C. Jackson, Donna L. Forrest, Man-Chiu Poon, Cynthia L. Toze, Michael J. Barnett

Publikováno v: Blood. 112(12)

Familial platelet disorder with propensity to myeloid malignancy (FPD/AML) is an autosomal dominant syndrome characterized by platelet abnormalities and a predisposition to myelodysplasia (MDS) and/or acute myeloid leukemia (AML). The disorder, cause

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::098e370786ebbf67eadc6df20fc6a402
https://pubmed.ncbi.nlm.nih.gov/18723428

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Five New Pedigrees with Inherited RUNX1 Mutations Causing Familial Platelet Disorder with Propensity to Myeloid Malignancy (FPD/AML)

Autor: Jude Fitzgibbon, T. Andrew Lister, Michael J. Barnett, John AL Yin, Anthony Macheta, Peter Johnson, Brian Leber, Gary D. Sinclair, Man-Chiu Poon, Shannon C Jackson, Clayton A. Smith, Donna L. Forrest, Anna Koochin, Cynthia L Toze, Carolyn J Owen

Publikováno v: Blood. 112:5067-5067

Familial platelet disorder with propensity to myeloid malignancy (FPD/AML) is an autosomal dominant syndrome characterised by platelet abnormalities and a predisposition to myelodysplasia (MDS) and/or acute myeloid leukemia (AML). The disorder, cause

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::be23b79a0dbeb0c246c278bcddc39ad8
https://doi.org/10.1182/blood.v112.11.5067.5067

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Should Patients with Myelodysplasia and/or Acute Myeloid Leukemia (MDS/AML) Be Screened for Inherited RUNX1 Mutations Prior to Sibling Donor Allografting?

Autor: T. Andrew, Cynthia J. Toze, Clayton A. Smith, Anthony Macheta, Donna L. Forrest, John A. Liu Yin, Carolyn Owen, Jude Fitzgibbon, Michael J. Barnett

Publikováno v: Blood. 110:5027-5027

Background Familial platelet disorder with propensity to myeloid malignancy (FPD/AML) is an autosomal dominant disease characterised by platelet abnormalities and risk of MDS/AML. FPD/AML results from germline mutations in RUNX1. The phenotype is het

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::867fe4f9e64f10004137d30b68234e9d
https://doi.org/10.1182/blood.v110.11.5027.5027

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