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Racial Disparities in Blood Pressure at Time of Acute Ischemic Stroke Presentation: A Population Study
Racial Disparities in Blood Pressure at Time of Acute Ischemic Stroke Presentation: A Population Study
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Racial Disparities in Blood Pressure at Time of Acute Ischemic Stroke Presentation: A Population Study

Aziz, Yasmin N ; Sucharew, Heidi ; Stanton, Robert J ; Alwell, Kathleen ; Ferioli, Simona ; Khatri, Pooja ; Adeoye, Opeolu ; Flaherty, Matthew L ; Mackey, Jason ; De Los Rios La Rosa, Felipe ; Martini, Sharyl R ; Mistry, Eva A ; Coleman, Elisheva ; Jasne, Adam S ; Slavin, Sabreena J ; Walsh, Kyle ; Star, Michael ; Ridha, Mohamed ; Ades, Laura M C ; Haverbusch, Mary ; Demel, Stacie L ; Woo, Daniel ; Kissela, Brett M ; Kleindorfer, Dawn O

Journal of the American Heart Association, 2024-05, Vol.13 (9), p.e032645 [Periódico revisado por pares]

England: John Wiley and Sons Inc

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2
Ectopia lentis phenotypes and the FBN1 gene
Ectopia lentis phenotypes and the FBN1 gene
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Ectopia lentis phenotypes and the FBN1 gene

Adès, Lesley C. ; Holman, Katherine J. ; Brett, Maggie S. ; Edwards, Matthew J. ; Bennetts, Bruce

American journal of medical genetics, 2004-04, Vol.126A (3), p.284-289 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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3
Predicting the HER2 status of breast cancer from basic histopathology data: an analysis of 1500 breast cancers as part of the HER2000 International Study
Predicting the HER2 status of breast cancer from basic histopathology data: an analysis of 1500 breast cancers as part of the HER2000 International Study
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Predicting the HER2 status of breast cancer from basic histopathology data: an analysis of 1500 breast cancers as part of the HER2000 International Study

Bilous, M ; Ades, C ; Armes, J ; Bishop, J ; Brown, R ; Cooke, B ; Cummings, M ; Farshid, G ; Field, A ; Morey, A ; McKenzie, P ; Raymond, W ; Robbins, P ; Tan, L

Breast (Edinburgh), 2003-04, Vol.12 (2), p.92-98 [Periódico revisado por pares]

Netherlands: Elsevier Ltd

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4
Ten novel FBN2 mutations in congenital contractural arachnodactyly: Delineation of the molecular pathogenesis and clinical phenotype
Ten novel FBN2 mutations in congenital contractural arachnodactyly: Delineation of the molecular pathogenesis and clinical phenotype
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Ten novel FBN2 mutations in congenital contractural arachnodactyly: Delineation of the molecular pathogenesis and clinical phenotype

Gupta, Prateek A. ; Putnam, Elizabeth A. ; Carmical, Sonya G. ; Kaitila, Ilkka ; Steinmann, Beat ; Child, Anne ; Danesino, Cesare ; Metcalfe, Kay ; Berry, Susan A. ; Chen, Emily ; Delorme, Catherine Vincent ; Thong, Meow-Keong ; Adès, Lesley C. ; Milewicz, Dianna M.

Human mutation, 2002-01, Vol.19 (1), p.39-48 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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5
The Cardiac Genetics Clinic: a model for multidisciplinary genomic medicine
The Cardiac Genetics Clinic: a model for multidisciplinary genomic medicine
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The Cardiac Genetics Clinic: a model for multidisciplinary genomic medicine

Zentner, Dominica ; Thompson, Tina N ; James, Paul A ; Trainer, Alison ; Adès, Lesley C ; Macciocca, Ivan ; Taylor, Jessica A ; Mann, Kirsty ; Bogwitz, Michael ; Lewis, Nigel ; Morgan, Natalie ; Vohra, Jitendra ; Winship, Ingrid

Medical journal of Australia, 2015-09, Vol.203 (6), p.261-261 [Periódico revisado por pares]

Australia

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6
Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands
Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands
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Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands

Faivre, L ; Collod-Beroud, G ; Child, A ; Callewaert, B ; Loeys, B L ; Binquet, C ; Gautier, E ; Arbustini, E ; Mayer, K ; Arslan-Kirchner, M ; Stheneur, C ; Kiotsekoglou, A ; Comeglio, P ; Marziliano, N ; Halliday, D ; Beroud, C ; Bonithon-Kopp, C ; Claustres, M ; Plauchu, H ; Robinson, P N ; Adès, L ; De Backer, J ; Coucke, P ; Francke, U ; De Paepe, A ; Boileau, C ; Jondeau, G

Journal of medical genetics, 2008-06, Vol.45 (6), p.384-390 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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7
Segregation of a novel FBN1 gene mutation, G1796E, with kyphoscoliosis and radiographic evidence of vertebral dysplasia in three generations
Segregation of a novel FBN1 gene mutation, G1796E, with kyphoscoliosis and radiographic evidence of vertebral dysplasia in three generations
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Segregation of a novel FBN1 gene mutation, G1796E, with kyphoscoliosis and radiographic evidence of vertebral dysplasia in three generations

Adès, Lesley C. ; Sreetharan, Darshikka ; Onikul, Ella ; Stockton, Vivienne ; Watson, Karen C. ; Holman, Katherine J.

American journal of medical genetics, 2002-05, Vol.109 (4), p.261-270

New York: Wiley Subscription Services, Inc., A Wiley Company

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8
Role of Reduced-Intensity Conditioning Allogeneic Hematopoietic Stem-Cell Transplantation in Older Patients With De Novo Myelodysplastic Syndromes: An International Collaborative Decision Analysis
Role of Reduced-Intensity Conditioning Allogeneic Hematopoietic Stem-Cell Transplantation in Older Patients With De Novo Myelodysplastic Syndromes: An International Collaborative Decision Analysis
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Role of Reduced-Intensity Conditioning Allogeneic Hematopoietic Stem-Cell Transplantation in Older Patients With De Novo Myelodysplastic Syndromes: An International Collaborative Decision Analysis

KORETH, John ; PIDALA, Joseph ; FENAUX, Pierre ; JADERSTEN, Martin ; HELLSTROM-LINDBERG, Eva ; GALE, Robert Peter ; BEACH, C. L ; LEE, Stephanie J ; HOROWITZ, Mary M ; GREENBERG, Peter L ; TALLMAN, Martin S ; DIPERSIO, John F ; PEREZ, Waleska S ; BUNJES, Donald ; WEISDORF, Daniel J ; CUTLER, Corey ; DEEG, H. Joachim ; GARCIA-MANERO, Guillermo ; MALCOVATI, Luca ; CAZZOLA, Mario ; PARK, Sophie ; ITZYKSON, Raphael ; ADES, Lionel

Journal of clinical oncology, 2013-07, Vol.31 (21), p.2662-2670 [Periódico revisado por pares]

Alexandria, VA: American Society of Clinical Oncology

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9
Empirical versus Preemptive Antifungal Therapy for High-Risk, Febrile, Neutropenic Patients: A Randomized, Controlled Trial
Empirical versus Preemptive Antifungal Therapy for High-Risk, Febrile, Neutropenic Patients: A Randomized, Controlled Trial
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Empirical versus Preemptive Antifungal Therapy for High-Risk, Febrile, Neutropenic Patients: A Randomized, Controlled Trial

Cordonnier, Catherine ; Pautas, Cécile ; Maury, Sébastien ; Vekhoff, Anne ; Farhat, Hassan ; Suarez, Felipe ; Dhédin, Nathalie ; Isnard, Francoise ; Ades, Lionel ; Kuhnowski, Frédérique ; Foulet, Françoise ; Kuentz, Mathieu ; Maison, Patrick ; Bretagne, Stéphane ; Schwarzinger, Michaël

Clinical infectious diseases, 2009-04, Vol.48 (8), p.1042-1051 [Periódico revisado por pares]

Oxford: The University of Chicago Press

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10
Impact of TET2 mutations on response rate to azacitidine in myelodysplastic syndromes and low blast count acute myeloid leukemias
Impact of TET2 mutations on response rate to azacitidine in myelodysplastic syndromes and low blast count acute myeloid leukemias
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Impact of TET2 mutations on response rate to azacitidine in myelodysplastic syndromes and low blast count acute myeloid leukemias

ITZYKSON, R ; KOSMIDER, O ; PREUDHOMME, C ; ADES, L ; FENAUX, P ; FONTENAY, M ; CLUZEAU, T ; MANSAT-DE MAS, V ; DREYFUS, F ; BEYNE-RAUZY, O ; QUESNEL, B ; VEY, N ; GELSI-BOYER, V ; RAYNAUD, S

Leukemia, 2011-07, Vol.25 (7), p.1147-1152 [Periódico revisado por pares]

Avenel, NJ: Nature Publishing Group

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