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ArticlesPeer ReviewedFull Text
Safety and Efficacy of Mitapivat in Pyruvate Kinase Deficiency
Author / Creator:Grace, Rachael F ; Rose, Christian ; Layton, D. Mark ; Galactéros, Frédéric ; Barcellini, Wilma ; Morton, D. Holmes ; van Beers, Eduard J ; Yaish, Hassan ; Ravindranath, Yaddanapudi ; Kuo, Kevin H.M ; Sheth, Sujit ; Kwiatkowski, Janet L ; Barbier, Ann J ; Bodie, Susan ; Silver, Bruce ; Hua, Lei ; Kung, Charles ; Hawkins, Peter ; Jouvin, Marie-Hélène ; Bowden, Chris ; Glader, Bertil
Publisher:United States: Massachusetts Medical Society
Journal title:The New England journal of medicine, 2019-09, Vol.381 (10), p.933-944
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Neonatal Hemolytic Jaundice: Morphologic Features of Erythrocytes That Will Help You Diagnose the Underlying Condition
Author / Creator:Christensen, Robert D. ; Yaish, Hassan M. ; Lemons, Richard S.
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Neonatology (Basel, Switzerland), 2014-01, Vol.105 (4), p.243-249
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Variations in Both α-Spectrin (SPTA1) and β-Spectrin (SPTB) in a Neonate with Prolonged Jaundice in a Family where Nine Individuals Had Hereditary Elliptocytosis
Author / Creator:Christensen, Robert D. ; Nussenzveig, Roberto H. ; Reading, N. Scott ; Agarwal, Archana M. ; Prchal, Josef T. ; Yaish, Hassan M.
Publisher:Basel, Switzerland
Journal title:Neonatology (Basel, Switzerland), 2014-01, Vol.105 (1), p.1-4
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Novel α-spectrin mutation in trans with α-spectrin causing severe neonatal jaundice from hereditary spherocytosis
Author / Creator:Nussenzveig, Roberto H ; Christensen, Robert D ; Prchal, Josef T ; Yaish, Hassan M ; Agarwal, Archana M
Publisher:Switzerland
Journal title:Neonatology (Basel, Switzerland), 2014-01, Vol.106 (4), p.355-357
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A de novo T73I Mutation in PTPN11 in a Neonate with Severe and Prolonged Congenital Thrombocytopenia and Noonan Syndrome
Author / Creator:Christensen, Robert D. ; Yaish, Hassan M. ; Leon, Eyby L. ; Sola-Visner, Martha C. ; Agrawal, Pankaj B.
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Neonatology (Basel, Switzerland), 2013-07, Vol.104 (1), p.1-5
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A Previously Unknown Mutation in the Pyruvate Kinase Gene (PKLR) Identified from a Neonate with Severe Jaundice
Author / Creator:Yaish, Hassan M. ; Nussenzveig, Roberto H. ; Agarwal, Archana M. ; Siddiqui, Abdul H. ; Christensen, Robert D.
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Neonatology (Basel, Switzerland), 2014-01, Vol.106 (2), p.140-142
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ArticlesPeer ReviewedFull Text
Mantle Cell Lymphoma Presenting with Unusual Morphology in an Adolescent Female: A Case Report and Review of the Literature
Author / Creator:Smock, Kristi J. ; Yaish, Hassan M. ; Cairo, Mitchell S. ; Lones, Mark A. ; Willmore-Payne, Carlynn ; Perkins, Sherrie L.
Publisher:Los Angeles, CA: SAGE Publications
Journal title:Pediatric and developmental pathology, 2007-09, Vol.10 (5), p.403-408
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Novel [alpha]-Spectrin Mutation in Trans with [alpha]-Spectrin LEPRA Causing Severe Neonatal Jaundice from Hereditary Spherocytosis
Author / Creator:Nussenzveig, Roberto H ; Christensen, Robert D ; Prchal, Josef T ; Yaish, Hassan M ; Agarwal, Archana M
Publisher:Basel: S. Karger AG
Journal title:Neonatology (Basel, Switzerland), 2014-11, Vol.106 (4), p.355
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Novel α-Spectrin Mutation in Trans with α-SpectrinLEPRA Causing Severe Neonatal Jaundice from Hereditary Spherocytosis
Author / Creator:Nussenzveig, Roberto H. ; Christensen, Robert D. ; Prchal, Josef T. ; Yaish, Hassan M. ; Agarwal, Archana M.
Publisher:Basel, Switzerland
Journal title:Neonatology (Basel, Switzerland), 2014-11, Vol.106 (4), p.355-357
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ArticlesPeer ReviewedFull Text
Variations in Both [alpha]-Spectrin (SPTA1) and [beta]-Spectrin (SPTB) in a Neonate with Prolonged Jaundice in a Family where Nine Individuals Had Hereditary Elliptocytosis
Author / Creator:Christensen, Robert D ; Nussenzveig, Roberto H ; Reading, N Scott ; Agarwal, Archana M ; Prchal, Josef T ; Yaish, Hassan M
Publisher:Basel: S. Karger AG
Journal title:Neonatology (Basel, Switzerland), 2014-12, Vol.105 (1), p.1-4
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ArticlesPeer ReviewedFull Text
Mantle Cell Lymphoma Presenting with Unusual Morphology in an Adolescent Female: A Case Report and Review of the Literature
Author / Creator:Smock, Kristi ; Yaish, Hassan ; Cairo, Mitchell ; Lones, Mark ; Willmore-Payne, Carlynn ; Perkins, Sherrie
Journal title:Pediatric and developmental pathology, 2006, Vol.preprint (2007), p.1
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ArticlesPeer ReviewedFull Text
Mitapivat versus Placebo for Pyruvate Kinase Deficiency
Author / Creator:Al-Samkari, Hanny ; Galactéros, Frédéric ; Glenthøj, Andreas ; Rothman, Jennifer A ; Andres, Oliver ; Grace, Rachael F ; Morado-Arias, Marta ; Layton, D. Mark ; Onodera, Koichi ; Verhovsek, Madeleine ; Barcellini, Wilma ; Chonat, Satheesh ; Judge, Malia P ; Zagadailov, Erin ; Xu, Rengyi ; Hawkins, Peter ; Beynon, Vanessa ; Gheuens, Sarah ; van Beers, Eduard J
Publisher:United States: Massachusetts Medical Society
Journal title:The New England journal of medicine, 2022-04, Vol.386 (15), p.1432-1442
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Safety and Efficacy of Mitapivat in Pyruvate Kinase Deficiency

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Neonatal Hemolytic Jaundice: Morphologic Features of Erythrocytes That Will Help You Diagnose the Underlying Condition

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Variations in Both α-Spectrin (SPTA1) and β-Spectrin (SPTB) in a Neonate with Prolonged Jaundice in a Family where Nine Individuals Had Hereditary Elliptocytosis

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Novel α-spectrin mutation in trans with α-spectrin causing severe neonatal jaundice from hereditary spherocytosis

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A de novo T73I Mutation in PTPN11 in a Neonate with Severe and Prolonged Congenital Thrombocytopenia and Noonan Syndrome

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A Previously Unknown Mutation in the Pyruvate Kinase Gene (PKLR) Identified from a Neonate with Severe Jaundice

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Mantle Cell Lymphoma Presenting with Unusual Morphology in an Adolescent Female: A Case Report and Review of the Literature

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Novel [alpha]-Spectrin Mutation in Trans with [alpha]-Spectrin LEPRA Causing Severe Neonatal Jaundice from Hereditary Spherocytosis

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Novel α-Spectrin Mutation in Trans with α-SpectrinLEPRA Causing Severe Neonatal Jaundice from Hereditary Spherocytosis

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Variations in Both [alpha]-Spectrin (SPTA1) and [beta]-Spectrin (SPTB) in a Neonate with Prolonged Jaundice in a Family where Nine Individuals Had Hereditary Elliptocytosis

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Mantle Cell Lymphoma Presenting with Unusual Morphology in an Adolescent Female: A Case Report and Review of the Literature

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Mitapivat versus Placebo for Pyruvate Kinase Deficiency

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