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Manuel D Carcao

Showing results (11-20 of 32) with videos related to

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Platelets|June 6, 2018
NBEAL2 mutations and bleeding in patients with gray platelet syndromeFred G Pluthero, Jorge Di Paola, Manuel D Carcao, et al.
Pediatric Blood & Cancer|March 23, 2011
Therapeutic consequences for misdiagnosis of type 2N von Willebrand diseaseMadhu Gupta, David Lillicrap, Ann Marie Stain, et al.
British Journal of Haematology|June 13, 2002
DDAVP challenge tests in boys with mild/moderate haemophilia AShoshana Revel-Vilk, Victor S Blanchette, Cathy Sparling, et al.
Pediatric Dermatology|July 31, 2019
Dieulafoy lesions and PHACE syndromeLukas Kieswetter, Thomas D Walters, Irene Lara-Corrales, et al.
Journal of Pediatric Hematology/Oncology|November 11, 2003
Desmopressin (DDAVP) responsiveness in children with von Willebrand diseaseShoshana Revel-Vilk, Markus Schmugge, Manuel D Carcao, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 1, 2023
Unravelling the effect of blood group on FVIII:C levels and response to DDAVP in 20 males with a single genotype (Twillingate Variant) causing Haemophilia AMichael Shu, Caroline Malcolmson, Vanessa Bouskill, et al.
British Journal of Haematology|December 21, 2002
Fcgamma receptor IIa and IIIa polymorphisms in childhood immune thrombocytopenic purpuraManuel D Carcao, Victor S Blanchette, Cindy D Wakefield, et al.
Hemoglobin|June 10, 2026
Hb F-SickKids (<i>HBG2</i>: C.308A > G): A Novel γ-Globin Variant Associated with Transient Neonatal CyanosisLandry E Nfonsam, Meredith Hanna, Lisa Nakamura, et al.
British Journal of Haematology|July 9, 2019
Abnormal fibrinolysis recognized by thromboelastography in a case of severe bleeding with normal coagulation and platelet function, leads to detection of a novel SERPINF2 variant causing severe alpha-2-antiplasmin deficiencyGrace Egan, Fred G Pluthero, Vanessa Bouskill, et al.
Paediatrics & Child Health|August 26, 2021
The use of rapamycin to treat vascular tumours and malformations: A single-centre experienceSoumitra Tole, Michelle Fantauzzi, Diana Cottingham, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Platelets|June 6, 2018
NBEAL2 mutations and bleeding in patients with gray platelet syndromeFred G Pluthero, Jorge Di Paola, Manuel D Carcao, et al.
Pediatric Blood & Cancer|March 23, 2011
Therapeutic consequences for misdiagnosis of type 2N von Willebrand diseaseMadhu Gupta, David Lillicrap, Ann Marie Stain, et al.
British Journal of Haematology|June 13, 2002
DDAVP challenge tests in boys with mild/moderate haemophilia AShoshana Revel-Vilk, Victor S Blanchette, Cathy Sparling, et al.
Pediatric Dermatology|July 31, 2019
Dieulafoy lesions and PHACE syndromeLukas Kieswetter, Thomas D Walters, Irene Lara-Corrales, et al.
Journal of Pediatric Hematology/Oncology|November 11, 2003
Desmopressin (DDAVP) responsiveness in children with von Willebrand diseaseShoshana Revel-Vilk, Markus Schmugge, Manuel D Carcao, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 1, 2023
Unravelling the effect of blood group on FVIII:C levels and response to DDAVP in 20 males with a single genotype (Twillingate Variant) causing Haemophilia AMichael Shu, Caroline Malcolmson, Vanessa Bouskill, et al.
British Journal of Haematology|December 21, 2002
Fcgamma receptor IIa and IIIa polymorphisms in childhood immune thrombocytopenic purpuraManuel D Carcao, Victor S Blanchette, Cindy D Wakefield, et al.
Hemoglobin|June 10, 2026
Hb F-SickKids (<i>HBG2</i>: C.308A > G): A Novel γ-Globin Variant Associated with Transient Neonatal CyanosisLandry E Nfonsam, Meredith Hanna, Lisa Nakamura, et al.
British Journal of Haematology|July 9, 2019
Abnormal fibrinolysis recognized by thromboelastography in a case of severe bleeding with normal coagulation and platelet function, leads to detection of a novel SERPINF2 variant causing severe alpha-2-antiplasmin deficiencyGrace Egan, Fred G Pluthero, Vanessa Bouskill, et al.
Paediatrics & Child Health|August 26, 2021
The use of rapamycin to treat vascular tumours and malformations: A single-centre experienceSoumitra Tole, Michelle Fantauzzi, Diana Cottingham, et al.
Pageof 4