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Rainer Rossi

Showing results (11-20 of 40) with videos related to

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Pediatric Blood & Cancer|June 7, 2006
Growth impairment after ifosfamide-induced nephrotoxicity in childrenWolfgang Stöhr, Ludwig Patzer, Marios Paulides, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|February 18, 2022
Günther Heller, Maurilio Gutzeit, Johannes Rauh, et al.
The Journal of Pediatrics|July 9, 2004
Variable clinical expression of an identical mutation in the ATP7A gene for Menkes disease/occipital horn syndrome in three affected males in a single familyBettina Borm, Lisbeth Birk Møller, Ingrid Hausser, et al.
Molecular and Cellular Pediatrics|July 3, 2020
Infant formula with cow's milk fat and prebiotics affects intestinal flora, but not the incidence of infections during infancy in a double-blind randomized controlled trialAntonia Nomayo, Andreas Schwiertz, Rainer Rossi, et al.
European Journal of Pediatrics|December 17, 2003
Prolonged survival in alveolar capillary dysplasia syndromeChristoph Licht, Sabine Schickendantz, Narayanswami Sreeram, et al.
American Journal of Human Genetics|February 20, 2004
Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase IChristian Kranz, Jonas Denecke, Ludwig Lehle, et al.
American Journal of Obstetrics and Gynecology|October 22, 2002
Rate and risk factors of hypoglycemia in large-for-gestational-age newborn infants of nondiabetic mothersUte M Schaefer-Graf, Rainer Rossi, Christoph Bührer, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|October 4, 2007
Hay-Wells syndrome in a child with mutation in the TP73L geneNatalie Garcia Bartels, Luitgard M Neumann, Anna Mleczko, et al.
European Journal of Endocrinology|May 15, 2009
The spectrum of phenotypes associated with mutations in steroidogenic factor 1 (SF-1, NR5A1, Ad4BP) includes severe penoscrotal hypospadias in 46,XY males without adrenal insufficiencyBirgit Köhler, Lin Lin, Inas Mazen, et al.
Thrombosis and Haemostasis|September 30, 2003
Homozygous and double heterozygous Factor V Leiden and Factor II G20210A genotypes predispose infants to thromboembolism but are not associated with an increase of foetal lossPatrick Hundsdoerfer, Barbara Vetter, Brigitte Stöver, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Pediatric Blood & Cancer|June 7, 2006
Growth impairment after ifosfamide-induced nephrotoxicity in childrenWolfgang Stöhr, Ludwig Patzer, Marios Paulides, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|February 18, 2022
Günther Heller, Maurilio Gutzeit, Johannes Rauh, et al.
The Journal of Pediatrics|July 9, 2004
Variable clinical expression of an identical mutation in the ATP7A gene for Menkes disease/occipital horn syndrome in three affected males in a single familyBettina Borm, Lisbeth Birk Møller, Ingrid Hausser, et al.
Molecular and Cellular Pediatrics|July 3, 2020
Infant formula with cow's milk fat and prebiotics affects intestinal flora, but not the incidence of infections during infancy in a double-blind randomized controlled trialAntonia Nomayo, Andreas Schwiertz, Rainer Rossi, et al.
European Journal of Pediatrics|December 17, 2003
Prolonged survival in alveolar capillary dysplasia syndromeChristoph Licht, Sabine Schickendantz, Narayanswami Sreeram, et al.
American Journal of Human Genetics|February 20, 2004
Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase IChristian Kranz, Jonas Denecke, Ludwig Lehle, et al.
American Journal of Obstetrics and Gynecology|October 22, 2002
Rate and risk factors of hypoglycemia in large-for-gestational-age newborn infants of nondiabetic mothersUte M Schaefer-Graf, Rainer Rossi, Christoph Bührer, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|October 4, 2007
Hay-Wells syndrome in a child with mutation in the TP73L geneNatalie Garcia Bartels, Luitgard M Neumann, Anna Mleczko, et al.
European Journal of Endocrinology|May 15, 2009
The spectrum of phenotypes associated with mutations in steroidogenic factor 1 (SF-1, NR5A1, Ad4BP) includes severe penoscrotal hypospadias in 46,XY males without adrenal insufficiencyBirgit Köhler, Lin Lin, Inas Mazen, et al.
Thrombosis and Haemostasis|September 30, 2003
Homozygous and double heterozygous Factor V Leiden and Factor II G20210A genotypes predispose infants to thromboembolism but are not associated with an increase of foetal lossPatrick Hundsdoerfer, Barbara Vetter, Brigitte Stöver, et al.
Pageof 4