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4G4G genotype of the plasminogen activator inhibitor‐1 promoter polymorphism associates with disseminated intravascular coagulation in children with systemic meningococcemia
4G4G genotype of the plasminogen activator inhibitor‐1 promoter polymorphism associates with disseminated intravascular coagulation in children with systemic meningococcemia
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4G4G genotype of the plasminogen activator inhibitor‐1 promoter polymorphism associates with disseminated intravascular coagulation in children with systemic meningococcemia

BINDER, A. ; ENDLER, G. ; MÜLLER, M. ; MANNHALTER, C. ; ZENZ, W.

Journal of thrombosis and haemostasis, 2007-10, Vol.5 (10), p.2049-2054 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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2
Aplastic anemia following hepatitis
Aplastic anemia following hepatitis
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Aplastic anemia following hepatitis

Schwarz, E ; Bachner, R L ; Diamond, L K

Pediatrics (Evanston), 1966-04, Vol.37 (4), p.681-683 [Periódico revisado por pares]

United States

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3
Assessment of an optimized manufacturing process for inactivated quadrivalent influenza vaccine: a phase III, randomized, double-blind, safety and immunogenicity study in children and adults
Assessment of an optimized manufacturing process for inactivated quadrivalent influenza vaccine: a phase III, randomized, double-blind, safety and immunogenicity study in children and adults
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Assessment of an optimized manufacturing process for inactivated quadrivalent influenza vaccine: a phase III, randomized, double-blind, safety and immunogenicity study in children and adults

Claeys, Carine ; Drame, Mamadou ; García-Sicilia, José ; Zaman, Khalequ ; Carmona, Alfonso ; Tran, Phu My ; Miranda, Mariano ; Martinón-Torres, Federico ; Thollot, Franck ; Horn, Michael ; Schwarz, Tino F ; Behre, Ulrich ; Merino, José M ; Sadowska-Krawczenko, Iwona ; Szymański, Henryk ; Schu, Peter ; Neumeier, Elisabeth ; Li, Ping ; Jain, Varsha K ; Innis, Bruce L

BMC infectious diseases, 2018-04, Vol.18 (1), p.186-13, Article 186 [Periódico revisado por pares]

England: BioMed Central Ltd

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4
Autoimmunity in Wiskott-Aldrich Syndrome: Risk Factors, Clinical Features, and Outcome in a Single-Center Cohort of 55 Patients
Autoimmunity in Wiskott-Aldrich Syndrome: Risk Factors, Clinical Features, and Outcome in a Single-Center Cohort of 55 Patients
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Autoimmunity in Wiskott-Aldrich Syndrome: Risk Factors, Clinical Features, and Outcome in a Single-Center Cohort of 55 Patients

Dupuis-Girod, Sophie ; Medioni, Jacques ; Haddad, Elie ; Quartier, Pierre ; Cavazzana-Calvo, Marina ; Le Deist, Francoise ; de Saint Basile, Genevieve ; Delaunay, Jean ; Schwarz, Klaus ; Casanova, Jean-Laurent ; Blanche, Stephane ; Fischer, Alain

Pediatrics (Evanston), 2003-05, Vol.111 (5), p.e622-e627 [Periódico revisado por pares]

United States: Am Acad Pediatrics

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5
Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin
Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin
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Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin

Seo, Aaron ; Ben-Harosh, Miri ; Sirin, Mehtap ; Stein, Jerry ; Dgany, Orly ; Kaplelushnik, Joseph ; Hoenig, Manfred ; Pannicke, Ulrich ; Lorenz, Myriam ; Schwarz, Klaus ; Stockklausner, Clemens ; Walsh, Tom ; Gulsuner, Suleyman ; Lee, Ming K. ; Sendamarai, Anoop ; Sanchez-Bonilla, Marilyn ; King, Mary-Claire ; Cario, Holger ; Kulozik, Andreas E. ; Debatin, Klaus-Michael ; Schulz, Ansgar ; Tamary, Hannah ; Shimamura, Akiko

Blood, 2017-08, Vol.130 (7), p.875-880 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Bone resorption in syndromes of the Ras/MAPK pathway
Bone resorption in syndromes of the Ras/MAPK pathway
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Bone resorption in syndromes of the Ras/MAPK pathway

Stevenson, DA ; Schwarz, EL ; Carey, JC ; Viskochil, DH ; Hanson, H ; Bauer, S ; Cindy Weng, H-Y ; Greene, T ; Reinker, K ; Swensen, J ; Chan, RJ ; Yang, F-C ; Senbanjo, L ; Yang, Z ; Mao, R ; Pasquali, M

Clinical genetics, 2011-12, Vol.80 (6), p.566-573 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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7
BRAF mutation is not predictive of long‐term outcome in papillary thyroid carcinoma
BRAF mutation is not predictive of long‐term outcome in papillary thyroid carcinoma
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BRAF mutation is not predictive of long‐term outcome in papillary thyroid carcinoma

Henke, Lauren E. ; Pfeifer, John D. ; Ma, Changquing ; Perkins, Stephanie M. ; DeWees, Todd ; El‐Mofty, Samir ; Moley, Jeffrey F. ; Nussenbaum, Brian ; Haughey, Bruce H. ; Baranski, Thomas J. ; Schwarz, Julie K. ; Grigsby, Perry W.

Cancer medicine (Malden, MA), 2015-06, Vol.4 (6), p.791-799 [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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8
Cerebral haemorrhage in long-term survivors of childhood acute lymphoblastic leukaemia
Cerebral haemorrhage in long-term survivors of childhood acute lymphoblastic leukaemia
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Cerebral haemorrhage in long-term survivors of childhood acute lymphoblastic leukaemia

HUMPL, T ; BRÜHL, K ; BOHL, J ; SCHWARZ, M ; STOETER, P ; GUTJAHR, P

European journal of pediatrics, 1997-05, Vol.156 (5), p.367-370 [Periódico revisado por pares]

Heidelberg: Springer

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9
Cerebral spinal fluid flow, venous drainage and spinal cord compression in achondroplastic children : impact of magnetic resonance findings for decompressive surgery at the cranio-cervical junction
Cerebral spinal fluid flow, venous drainage and spinal cord compression in achondroplastic children : impact of magnetic resonance findings for decompressive surgery at the cranio-cervical junction
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Cerebral spinal fluid flow, venous drainage and spinal cord compression in achondroplastic children : impact of magnetic resonance findings for decompressive surgery at the cranio-cervical junction

BRÜHL, Klaus ; STOETER, Peter ; WIETEK, Beate ; SCHWARZ, Manfred ; HUMPL, Tilman ; SCHUMACHER, Reinhard ; SPRANGER, Jürgen

European journal of pediatrics, 2001, Vol.160 (1), p.10-20 [Periódico revisado por pares]

Heidelberg: Springer

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10
Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene : a cystic fibrosis mutation of slavic origin common in Central and East Europe
Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene : a cystic fibrosis mutation of slavic origin common in Central and East Europe
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Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene : a cystic fibrosis mutation of slavic origin common in Central and East Europe

DÖRK, T ; MACEK, M. JR ; ZEMKOVA, D ; GINTER, E ; PETROVA, N. V ; IVASCHENKO, T ; BARANOV, V ; WITT, M ; POGORZELSKI, A ; BAL, J ; ZEKANOWSKY, C ; WAGNER, K ; MEKUS, F ; STUHRMANN, M ; BAUER, I ; SEYDEWITZ, H. H ; NEUMANN, T ; JAKUBICZKA, S ; KRAUS, C ; THAMM, B ; NECHIPORENKO, M ; LIVSHITS, L ; MOSSE, N ; TÜMMLER, B ; TSUKERMAN, G ; KADASI, L ; RAVNIK-GLAVAC, M ; GLAVAC, D ; KOMEL, R ; VOUK, K ; KUCINSKAS, V ; KRUMINA, A ; TEDER, M ; KOCHEVA, S ; TZOUNTZOURIS, J ; EFREMOV, G. D ; ONAY, T ; KIRDAR, B ; MALONE, G ; SCHWARZ, M ; ZHAOQING ZHOU ; FRIEDMAN, K. J ; CARLES, S ; CLAUSTRES, M ; BOZON, D ; CASALS, T ; VERLINGUE, C ; FEREC, C ; TZETIS, M ; KANAVAKIS, E ; CUPPENS, H ; BOMBIERI, C ; PIGNATTI, P. F ; SANGIUOLO, F ; JORDANOVA, A ; KUSIC, J ; KREBSOVA, A ; KOUDOVA, M ; SAKMARYOVA, I. SR ; VAVROVA, V

Human genetics, 2000-03, Vol.106 (3), p.259-268 [Periódico revisado por pares]

Heidelberg: Springer

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