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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 30, 2022
Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in France
L Levaillant, F Huet, P Bretones, et al.
The Journal of Pathology
|
October 24, 2001
Expression of angiogenesis-related molecules in plexiform lesions in severe pulmonary hypertension: evidence for a process of disordered angiogenesis
R M Tuder, M Chacon, L Alger, et al.
European Journal of Endocrinology
|
February 19, 2014
Unexpected high frequency of skeletal dysplasia in idiopathic short stature and small for gestational age patients
I Flechtner, K Lambot-Juhan, R Teissier, et al.
Prenatal Diagnosis
|
October 20, 2000
Management of fetal thyroid goitres: a report of 11 cases in a single perinatal unit
J L Volumenie, M Polak, J Guibourdenche, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 2, 2013
Childhood craniopharyngioma: hypothalamus-sparing surgery decreases the risk of obesity
E Elowe-Gruau, J Beltrand, R Brauner, et al.
Journal of Medical Genetics
|
November 6, 2001
Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritance
L Faivre, M Le Merrer, C Baumann, et al.
Journal of the Royal Society, Interface
|
November 27, 2008
Stem cell bioprocessing: fundamentals and principles
Mark R Placzek, I-Ming Chung, Hugo M Macedo, et al.
European Journal of Endocrinology
|
March 26, 2014
Characterization and prevalence of severe primary IGF1 deficiency in a large cohort of French children with short stature
R Teissier, I Flechtner, A Colmenares, et al.
Journal of the Society for Gynecologic Investigation
|
January 1, 1996
International, collaborative experience of 1789 patients having multifetal pregnancy reduction: a plateauing of risks and outcomes
M I Evans, M Dommergues, R J Wapner, et al.
Clinical Genetics
|
October 11, 2007
Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates
W W J de Leng, M Jansen, R Carvalho, et al.
Page
of 99
Search research articles
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Showing results (971-980 of 984) with videos related to
Sort By:
Page
of 99
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 30, 2022
Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in France
L Levaillant, F Huet, P Bretones, et al.
The Journal of Pathology
|
October 24, 2001
Expression of angiogenesis-related molecules in plexiform lesions in severe pulmonary hypertension: evidence for a process of disordered angiogenesis
R M Tuder, M Chacon, L Alger, et al.
European Journal of Endocrinology
|
February 19, 2014
Unexpected high frequency of skeletal dysplasia in idiopathic short stature and small for gestational age patients
I Flechtner, K Lambot-Juhan, R Teissier, et al.
Prenatal Diagnosis
|
October 20, 2000
Management of fetal thyroid goitres: a report of 11 cases in a single perinatal unit
J L Volumenie, M Polak, J Guibourdenche, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 2, 2013
Childhood craniopharyngioma: hypothalamus-sparing surgery decreases the risk of obesity
E Elowe-Gruau, J Beltrand, R Brauner, et al.
Journal of Medical Genetics
|
November 6, 2001
Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritance
L Faivre, M Le Merrer, C Baumann, et al.
Journal of the Royal Society, Interface
|
November 27, 2008
Stem cell bioprocessing: fundamentals and principles
Mark R Placzek, I-Ming Chung, Hugo M Macedo, et al.
European Journal of Endocrinology
|
March 26, 2014
Characterization and prevalence of severe primary IGF1 deficiency in a large cohort of French children with short stature
R Teissier, I Flechtner, A Colmenares, et al.
Journal of the Society for Gynecologic Investigation
|
January 1, 1996
International, collaborative experience of 1789 patients having multifetal pregnancy reduction: a plateauing of risks and outcomes
M I Evans, M Dommergues, R J Wapner, et al.
Clinical Genetics
|
October 11, 2007
Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates
W W J de Leng, M Jansen, R Carvalho, et al.
Page
of 99