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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
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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3
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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4
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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5
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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6
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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7
Clinical aspects and prognosis of ependymoma in infants and children. A single institution experience
Clinical aspects and prognosis of ependymoma in infants and children. A single institution experience
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Clinical aspects and prognosis of ependymoma in infants and children. A single institution experience

Humpl, T ; Neuser, H ; Brühl, K ; Bartels, U ; Schwarz, M ; Gutjahr, P

Child's nervous system, 2001-04, Vol.17 (4-5), p.246-251 [Periódico revisado por pares]

Germany

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8
Common brain disorders are associated with heritable patterns of apparent aging of the brain
Common brain disorders are associated with heritable patterns of apparent aging of the brain
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Common brain disorders are associated with heritable patterns of apparent aging of the brain

Kaufmann, Tobias ; van der Meer, Dennis ; Doan, Nhat Trung ; Schwarz, Emanuel ; Lund, Martina J ; Agartz, Ingrid ; Alnæs, Dag ; Barch, Deanna M ; Baur-Streubel, Ramona ; Bertolino, Alessandro ; Bettella, Francesco ; Beyer, Mona K ; Bøen, Erlend ; Borgwardt, Stefan ; Brandt, Christine L ; Buitelaar, Jan ; Celius, Elisabeth G ; Cervenka, Simon ; Conzelmann, Annette ; Córdova-Palomera, Aldo ; Dale, Anders M ; de Quervain, Dominique J F ; Di Carlo, Pasquale ; Djurovic, Srdjan ; Dørum, Erlend S ; Eisenacher, Sarah ; Elvsåshagen, Torbjørn ; Espeseth, Thomas ; Fatouros-Bergman, Helena ; Flyckt, Lena ; Franke, Barbara ; Frei, Oleksandr ; Haatveit, Beathe ; Håberg, Asta K ; Harbo, Hanne F ; Hartman, Catharina A ; Heslenfeld, Dirk ; Hoekstra, Pieter J ; Høgestøl, Einar A ; Jernigan, Terry L ; Jonassen, Rune ; Jönsson, Erik G ; Kirsch, Peter ; Kłoszewska, Iwona ; Kolskår, Knut K ; Landrø, Nils Inge ; Le Hellard, Stephanie ; Lesch, Klaus-Peter ; Lovestone, Simon ; Lundervold, Arvid ; Lundervold, Astri J ; Maglanoc, Luigi A ; Malt, Ulrik F ; Mecocci, Patrizia ; Melle, Ingrid ; Meyer-Lindenberg, Andreas ; Moberget, Torgeir ; Norbom, Linn B ; Nordvik, Jan Egil ; Nyberg, Lars ; Oosterlaan, Jaap ; Papalino, Marco ; Papassotiropoulos, Andreas ; Pauli, Paul ; Pergola, Giulio ; Persson, Karin ; Richard, Geneviève ; Rokicki, Jaroslav ; Sanders, Anne-Marthe ; Selbæk, Geir ; Shadrin, Alexey A ; Smeland, Olav B ; Soininen, Hilkka ; Sowa, Piotr ; Steen, Vidar M ; Tsolaki, Magda ; Ulrichsen, Kristine M ; Vellas, Bruno ; Wang, Lei ; Westman, Eric ; Ziegler, Georg C ; Zink, Mathias ; Andreassen, Ole A ; Westlye, Lars T

Nature neuroscience, 2019-10, Vol.22 (10), p.1617-1623 [Periódico revisado por pares]

United States: Nature Publishing Group

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9
Definition of a critical T cell threshold for prevention of GVHD after HLA non-identical PBPC transplantation in children
Definition of a critical T cell threshold for prevention of GVHD after HLA non-identical PBPC transplantation in children
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Definition of a critical T cell threshold for prevention of GVHD after HLA non-identical PBPC transplantation in children

MÜLLER, S ; SCHULZ, A ; REISS, U ; SCHWARZ, K ; SCHREINER, T ; WIESNETH, M ; DEBATIN, K.-M ; FRIEDRICH, W

Bone marrow transplantation (Basingstoke), 1999-09, Vol.24 (6), p.575-581 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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10
Diagnostic value of CK-MB isoenzyme determinations in children with craniocerebral injuries and polytrauma
Diagnostic value of CK-MB isoenzyme determinations in children with craniocerebral injuries and polytrauma
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Diagnostic value of CK-MB isoenzyme determinations in children with craniocerebral injuries and polytrauma

Stopfkuchen, H ; Schranz, D ; Salzmann, G ; Jüngst, B K ; Wiss, M ; Schwarz, M

Monatsschrift Kinderheilkunde, 1984-08, Vol.132 (8), p.594-599 [Periódico revisado por pares]

Germany

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