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Paris-Trousseau Thrombocytopenia

Known as: Paris Trousseau Thrombocytopenia, Disorder, 11q23 Deletion, Thrombocytopenia, Paris-Trousseau 
A component of Jacobsen Syndrome linked to FLI1 gene at 11q23.
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

Jacobsen Distal 11q Deletion Syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Congenital Toxoplasmosis in France and the United States: One Parasite, Two Diverging Approaches
1 Hospices Civils de Lyon, Institut de Parasitologie et mycologie médicale, Hôpital de la Croix Rousse, Lyon, France, 2… Expand
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2015
2015
Paris-Trousseau thrombocytopenia is phenocopied by the autosomal recessive inheritance of a DNA-binding domain mutation in FLI1.
Hemizygous deletion of a variable region on chromosome 11q containing FLI1 causes an inherited platelet-related bleeding disorder… Expand
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Review
2014
Review
2014
Cell therapy for bone repair.
When natural bone repair mechanisms fail, autologous bone grafting is the current standard of care. The osteogenic cells and bone… Expand
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2014
2014
Early-onset Behr syndrome due to compound heterozygous mutations in OPA1.
Sir, The Behr syndrome (MIM#210000) is characterized by the association of early-onset optic atrophy with spinocerebellar… Expand
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2011
2011
Remuneração e características do trabalho docente no Brasil: um aporte
O objetivo do artigo e descrever algumas caracteristicas do trabalho docente e comparar a remuneracao dos professores a de outros… Expand
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Review
2008
Review
2008
Clinical practice. Hypoparathyroidism.
Copyright © 2008 Massachusetts Medical Society. A 58-year-old man is found on laboratory testing to have a serum calcium level of… Expand
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2008
2008
Cochlear implant magnet displacement during magnetic resonance imaging.
OBJECTIVE Magnet displacement is a rare but possible complication in patients with cochlear implants. We report 1 case in a young… Expand
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Highly Cited
2005
Highly Cited
2005
Early childhood risk factors associated with type 1 diabetes – is gender important?
Abstract.Background: The incidence of childhood diabetes is increasing in Denmark as in the rest of the world. The aim of this… Expand
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Highly Cited
2002
Highly Cited
2002
Interventricular and intraventricular dyssynchrony in idiopathic dilated cardiomyopathy: a prognostic study with fourier phase analysis of radionuclide angioscintigraphy.
OBJECTIVES The study evaluated the prognostic value of interventricular and intraventricular dyssynchrony in idiopathic dilated… Expand
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1999
1999
Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait.
van der Woude syndrome (vWS, MIM 119300) is a rare autosomal dominant clefting condition with cardinal features of mucous cysts… Expand
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