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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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12
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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13
Changes in Distribution of Severe Neurologic Involvement in US Pediatric Inpatients With COVID-19 or Multisystem Inflammatory Syndrome in Children in 2021 vs 2020
Changes in Distribution of Severe Neurologic Involvement in US Pediatric Inpatients With COVID-19 or Multisystem Inflammatory Syndrome in Children in 2021 vs 2020
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Changes in Distribution of Severe Neurologic Involvement in US Pediatric Inpatients With COVID-19 or Multisystem Inflammatory Syndrome in Children in 2021 vs 2020

LaRovere, Kerri L ; Poussaint, Tina Y ; Young, Cameron C ; Newhams, Margaret M ; Kucukak, Suden ; Irby, Katherine ; Kong, Michele ; Schwartz, Stephanie P ; Walker, Tracie C ; Bembea, Melania M ; Wellnitz, Kari ; Havlin, Kevin M ; Cvijanovich, Natalie Z ; Hall, Mark W ; Fitzgerald, Julie C ; Schuster, Jennifer E ; Hobbs, Charlotte V ; Halasa, Natasha B ; Singh, Aalok R ; Mack, Elizabeth H ; Bradford, Tamara T ; Gertz, Shira J ; Schwarz, Adam J ; Typpo, Katri V ; Loftis, Laura L ; Giuliano, John S ; Horwitz, Steven M ; Biagas, Katherine V ; Clouser, Katharine N ; Rowan, Courtney M ; Maddux, Aline B ; Soma, Vijaya L ; Babbitt, Christopher J ; Aguiar, Cassyanne L ; Kolmar, Amanda R ; Heidemann, Sabrina M ; Harvey, Helen ; Zambrano, Laura D ; Campbell, Angela P ; Randolph, Adrienne G

JAMA neurology, 2023-01, Vol.80 (1), p.91-98 [Periódico revisado por pares]

United States: American Medical Association

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14
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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15
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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16
Clinical impact of MRI in acute wrist fractures
Clinical impact of MRI in acute wrist fractures
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Clinical impact of MRI in acute wrist fractures

Mack, Martin G ; Keim, Sabine ; Balzer, Jörn O ; Schwarz, Wolfram ; Hochmuth, Kathrin ; Windolf, Joachim ; Vogl, Thomas J

European radiology, 2003-03, Vol.13 (3), p.612-617 [Periódico revisado por pares]

Germany: Springer Nature B.V

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17
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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18
Comparison of different substances for subureteric injection in the management of vesicoureteric reflux in children
Comparison of different substances for subureteric injection in the management of vesicoureteric reflux in children
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Comparison of different substances for subureteric injection in the management of vesicoureteric reflux in children

Pelletier, A K ; Anderson, P A M ; Schwarz, R D

Canadian journal of urology, 2005-08, Vol.12 (4), p.2774-2777 [Periódico revisado por pares]

Canada

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19
Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation
Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation
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Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation

Heimpel, Hermann ; Schwarz, Klaus ; Ebnöther, Monika ; Goede, Jeroen S. ; Heydrich, Detlev ; Kamp, Torsten ; Plaumann, Lothar ; Rath, Bettina ; Roessler, Jochen ; Schildknecht, Otto ; Schmid, Mathias ; Wuillemin, Walter ; Einsiedler, Beate ; Leichtle, Rosi ; Tamary, Hannah ; Kohne, Elisabeth

Blood, 2006-01, Vol.107 (1), p.334-340 [Periódico revisado por pares]

Washington, DC: Elsevier Inc

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20
CYP11B1 mutations causing congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
CYP11B1 mutations causing congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
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CYP11B1 mutations causing congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

GELEY, S ; KAPLERAI, K ; KOFLER, R ; JÖHRER, K ; PETER, M ; GLATZL, J ; VIERHAPPER, H ; SCHWARZ, S ; HELMBERG, A ; SIPPELL, W. G ; WHITE, P. C

The journal of clinical endocrinology and metabolism, 1996-08, Vol.81 (8), p.2896-2901 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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