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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.
2014
2014
Plan d’action en cas de réaction accidentelle dans l’allergie alimentaire chez l’enfant : position du groupe de travail « allergie alimentaire » sous l’égide de la Société française d’allergologie
2014
2014
Thromboses itératives de pontages artériels et cancer : à propos de trois cas
Review
2013
Review
2013
Brief update on hemodynamic responses in animal models of neonatal stroke and hypoxia–ischemia
Review
2011
Review
2011
Tacrolimus adverse events in transplant recipients with diarrhoea or calcium channel blockers: Systematic review
1 Centre for Statistics in Medicine, University of Oxford, Oxford, United-Kingdom. 2 Department of Pediatric Nephrology, Armand… 
2010
2010
Polysaccharide pneumococcal vaccination of nephrotic children at disease onset–long-term data
Sirs, Patients with nephrotic syndrome (NS) are at risk of developing pneumococcal infections, such as peritonitis, pneumonia… 
2010
2010
First‐trimester molecular prenatal diagnosis of a thanatophoric dysplasia
Sophie Delahaye1, Jonathan Rosenblatt1, Jean-Marc Costa2, Anne Bazin3, Jean-Louis Bénifla1 and Jean-Marie Jouannic1* 1Service de… 
Review
2008
Review
2008
Hyperinflammation in airways of cystic fibrosis patients: what’s new?
Annick Clement, MD, PhD Inserm, UMR-S U893, UPMC, Paris 6, AP-HP, Hôpital Trousseau, Pediatric Pulmonary Department, 26 Avenue du… 
2005
2005
Armand Trousseau, die Phlegmasia alba und das Magenkarzinom
Zusammenfassung Armand Trousseau (1801–1867) gehörte zu den ganz großen Ärzten unseres Kulturkreises. Er betrachtete die Medizin… 
2001
2001
Lithiase biliaire chez l’enfant drépanocytaire : expérience d’un hôpital pédiatrique parisien
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… 
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