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Helvetica Paediatrica Acta
|
January 1, 1979
Unilateral galactocoele in a male infant
M Vanderschueren-Lodeweyckx, M L Gielen, E Eggermont, et al.
Neuropediatrics
|
August 1, 1984
Gamma-aminobutyric acid-transaminase deficiency: a newly recognized inborn error of neurotransmitter metabolism
J Jaeken, P Casaer, P de Cock, et al.
Helvetica Paediatrica Acta
|
March 1, 1973
A hyperlipemia syndrome in infancy with rapidly fatal evolution
J Jaeken, M Casteels-van Daele, L Harvengt, et al.
Helvetica Paediatrica Acta
|
August 1, 1984
The thyroid-system function in preterm infants of postmenstrual ages of 31 weeks or less: evidence for a "transient lazy thyroid system"
E Eggermont, M Vanderschueren-Lodeweyckx, P De Nayer, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
June 1, 1993
Posterior fossa dermoid cyst associated with dermal fistula: report of 2 cases and review of the literature
J Goffin, C Plets, F Van Calenbergh, et al.
European Journal of Pediatrics
|
October 1, 1981
A boy with Leydig cell tumour and precocious puberty: ultrasonography as a diagnostic aid
M M Ilondo, F van den Mooter, G Marchal, et al.
The Journal of Pediatrics
|
November 1, 1988
Heparin plus dipyridamole in childhood hemolytic-uremic syndrome: a prospective, randomized study
R Van Damme-Lombaerts, W Proesmans, B Van Damme, et al.
Pediatric Research
|
January 1, 1981
Clinical and biochemical findings before and after portacaval shunt in a girl with type Ib glycogen storage disease
L Corbeel, L Hue, B Lederer, et al.
Acta Paediatrica Belgica
|
January 1, 1978
Familial deficiency of granulocyte bactericidal capacity associated with growth retardation
L Corbeel, R S Weening, D Roos, et al.
Human Genetics
|
January 25, 1979
A new chromosome anomaly in acute lymphoblastic leukemia (ALL)
H Van den Berghe, G David, A Broeckaert-Van Orshoven, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 102) with videos related to
Sort By:
Page
of 11
Helvetica Paediatrica Acta
|
January 1, 1979
Unilateral galactocoele in a male infant
M Vanderschueren-Lodeweyckx, M L Gielen, E Eggermont, et al.
Neuropediatrics
|
August 1, 1984
Gamma-aminobutyric acid-transaminase deficiency: a newly recognized inborn error of neurotransmitter metabolism
J Jaeken, P Casaer, P de Cock, et al.
Helvetica Paediatrica Acta
|
March 1, 1973
A hyperlipemia syndrome in infancy with rapidly fatal evolution
J Jaeken, M Casteels-van Daele, L Harvengt, et al.
Helvetica Paediatrica Acta
|
August 1, 1984
The thyroid-system function in preterm infants of postmenstrual ages of 31 weeks or less: evidence for a "transient lazy thyroid system"
E Eggermont, M Vanderschueren-Lodeweyckx, P De Nayer, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
June 1, 1993
Posterior fossa dermoid cyst associated with dermal fistula: report of 2 cases and review of the literature
J Goffin, C Plets, F Van Calenbergh, et al.
European Journal of Pediatrics
|
October 1, 1981
A boy with Leydig cell tumour and precocious puberty: ultrasonography as a diagnostic aid
M M Ilondo, F van den Mooter, G Marchal, et al.
The Journal of Pediatrics
|
November 1, 1988
Heparin plus dipyridamole in childhood hemolytic-uremic syndrome: a prospective, randomized study
R Van Damme-Lombaerts, W Proesmans, B Van Damme, et al.
Pediatric Research
|
January 1, 1981
Clinical and biochemical findings before and after portacaval shunt in a girl with type Ib glycogen storage disease
L Corbeel, L Hue, B Lederer, et al.
Acta Paediatrica Belgica
|
January 1, 1978
Familial deficiency of granulocyte bactericidal capacity associated with growth retardation
L Corbeel, R S Weening, D Roos, et al.
Human Genetics
|
January 25, 1979
A new chromosome anomaly in acute lymphoblastic leukemia (ALL)
H Van den Berghe, G David, A Broeckaert-Van Orshoven, et al.
Page
of 11