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Developmental Medicine and Child Neurology
|
June 28, 2003
Late sequelae of low birthweight: mediators of poor school performance at 11 years
Diana Weindrich, Christine Jennen-Steinmetz, Manfred Laucht, et al.
Journal of Medical Microbiology
|
May 1, 1994
Variants of Shiga-like toxin II constitute a major toxin component in Escherichia coli O157 strains from patients with haemolytic uraemic syndrome
H Rüssmann, H Schmidt, J Heesemann, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie
|
July 5, 2007
[Dopaminergic polymorphisms and regulatory problems in infancy]
Katja Becker, Mahha El-Faddagh, Martin H Schmidt, et al.
Injury
|
October 18, 2007
Advances in the treatment of intracapsular hip fractures in the elderly
Ross K Leighton, Andrew H Schmidt, Pamela Collier, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie
|
June 9, 2004
[Typical benign epilepsy potentials in childhood (Rolandic spikes)--neurobiological and neuropsychological symptoms and their clinical significance in child and adolescent psychiatry]
M Holtmann, K Becker, M el-Faddagh, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie
|
March 3, 2004
[How effective are interventions in children and adolescents with antisocial behavior? A utilization study]
A Wagner, C Jennen-Steinmetz, C Göpel, et al.
Anaesthesia and Intensive Care
|
March 3, 2010
Difficult double-lumen tube placement due to laryngeal web
M H Schmidt, R H Riley, G Y K Hee
Free Radical Research Communications
|
January 1, 1986
H2O2 formation during nucleotide degradation in the hypoxic rat liver: a quantitative approach
W Siems, H Schmidt, M Müller, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 1, 1991
Microheterogeneity of urinary albumin and tubular proteinuria in juvenile diabetes mellitus
M Ries, K Schärer, R Wartha, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 5, 2009
Congenital hypothyroidism caused by a novel homozygous mutation in the thyroid peroxidase gene
O Fuchs, N Pfarr, J Pohlenz, et al.
Page
of 363
Search research articles
Search
Showing results (1291-1300 of 3,630) with videos related to
Sort By:
Page
of 363
Developmental Medicine and Child Neurology
|
June 28, 2003
Late sequelae of low birthweight: mediators of poor school performance at 11 years
Diana Weindrich, Christine Jennen-Steinmetz, Manfred Laucht, et al.
Journal of Medical Microbiology
|
May 1, 1994
Variants of Shiga-like toxin II constitute a major toxin component in Escherichia coli O157 strains from patients with haemolytic uraemic syndrome
H Rüssmann, H Schmidt, J Heesemann, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie
|
July 5, 2007
[Dopaminergic polymorphisms and regulatory problems in infancy]
Katja Becker, Mahha El-Faddagh, Martin H Schmidt, et al.
Injury
|
October 18, 2007
Advances in the treatment of intracapsular hip fractures in the elderly
Ross K Leighton, Andrew H Schmidt, Pamela Collier, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie
|
June 9, 2004
[Typical benign epilepsy potentials in childhood (Rolandic spikes)--neurobiological and neuropsychological symptoms and their clinical significance in child and adolescent psychiatry]
M Holtmann, K Becker, M el-Faddagh, et al.
Zeitschrift Fur Kinder- Und Jugendpsychiatrie Und Psychotherapie
|
March 3, 2004
[How effective are interventions in children and adolescents with antisocial behavior? A utilization study]
A Wagner, C Jennen-Steinmetz, C Göpel, et al.
Anaesthesia and Intensive Care
|
March 3, 2010
Difficult double-lumen tube placement due to laryngeal web
M H Schmidt, R H Riley, G Y K Hee
Free Radical Research Communications
|
January 1, 1986
H2O2 formation during nucleotide degradation in the hypoxic rat liver: a quantitative approach
W Siems, H Schmidt, M Müller, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 1, 1991
Microheterogeneity of urinary albumin and tubular proteinuria in juvenile diabetes mellitus
M Ries, K Schärer, R Wartha, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 5, 2009
Congenital hypothyroidism caused by a novel homozygous mutation in the thyroid peroxidase gene
O Fuchs, N Pfarr, J Pohlenz, et al.
Page
of 363