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R Brauner

Showing results (181-190 of 189) with videos related to

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Archives of Disease in Childhood|January 6, 1999
Long-term follow up of 69 patients treated for optic pathway tumours before the chemotherapy eraC Cappelli, J Grill, M Raquin, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndromeS Hadj-Rabia, R Salomon, A Pelet, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarismF Castinetti, A Saveanu, R Reynaud, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 1, 2005
A nationwide study of granulosa cell tumors in pre- and postpubertal girls: missed diagnosis of endocrine manifestations worsens prognosisN Kalfa, C Patte, D Orbach, et al.
The Journal of Clinical Endocrinology and Metabolism|May 2, 2013
Childhood craniopharyngioma: hypothalamus-sparing surgery decreases the risk of obesityE Elowe-Gruau, J Beltrand, R Brauner, et al.
Hormone Research|December 5, 1998
Androgens and fetal growthF de Zegher, I Francois, A L Boehmer, et al.
Neuro-Chirurgie|September 19, 2008
[Childhood cerebral tumors: morbidity and follow-up into adulthood]J Grill, S Puget, E De Carli, et al.
Journal of Medical Genetics|June 17, 2003
Spectrum of NSD1 mutations in Sotos and Weaver syndromesM Rio, L Clech, J Amiel, et al.
Endocrine Research|January 26, 2005
A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutationsS Vallette-Kasic, A M Pulichino, M Gueydan, et al.
Pageof 19

Showing results (181-190 of 189) with videos related to

Sort By:
Pageof 19
You have reached the last page of results.This site can display upto 189 results.
Archives of Disease in Childhood|January 6, 1999
Long-term follow up of 69 patients treated for optic pathway tumours before the chemotherapy eraC Cappelli, J Grill, M Raquin, et al.
European Journal of Human Genetics : EJHG|August 22, 2000
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndromeS Hadj-Rabia, R Salomon, A Pelet, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarismF Castinetti, A Saveanu, R Reynaud, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 1, 2005
A nationwide study of granulosa cell tumors in pre- and postpubertal girls: missed diagnosis of endocrine manifestations worsens prognosisN Kalfa, C Patte, D Orbach, et al.
The Journal of Clinical Endocrinology and Metabolism|May 2, 2013
Childhood craniopharyngioma: hypothalamus-sparing surgery decreases the risk of obesityE Elowe-Gruau, J Beltrand, R Brauner, et al.
Hormone Research|December 5, 1998
Androgens and fetal growthF de Zegher, I Francois, A L Boehmer, et al.
Neuro-Chirurgie|September 19, 2008
[Childhood cerebral tumors: morbidity and follow-up into adulthood]J Grill, S Puget, E De Carli, et al.
Journal of Medical Genetics|June 17, 2003
Spectrum of NSD1 mutations in Sotos and Weaver syndromesM Rio, L Clech, J Amiel, et al.
Endocrine Research|January 26, 2005
A neonatal form of isolated ACTH deficiency frequently associated with Tpit gene mutationsS Vallette-Kasic, A M Pulichino, M Gueydan, et al.
Pageof 19