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Raquel Corripio

Showing results (1-10 of 43) with videos related to

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BMJ Case Reports|April 6, 2021
Vaginal bleeding in a misdiagnosed Mayer-Rokitansky-Küster-Hauser syndromeMireia Tugues, Bernardo Nuñez, Raquel Corripio
The American Journal of Case Reports|December 19, 2021
A 10-Year-Old Boy with Short Stature and Microcephaly, Diagnosed with Moyamoya Syndrome and Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II)Aurora Eslava, Montserrat Garcia-Puig, Raquel Corripio
BMJ Case Reports|February 2, 2013
Pseudohypoaldosteronism without nephropathy masking salt-wasting congenital adrenal hyperplasia genetically confirmedCarla Balcells, Teresa Gili, Jacobo Pérez, et al.
BMJ Case Reports|July 24, 2013
Disorder of sex development as a diagnostic clue in the first Spanish known newborn with P450 oxidoreductase deficiencyDunia Sánchez-Garvín, Sonia Albaladejo, Begoña Ezquieta, et al.
Journal of Clinical Medicine|March 25, 2022
Cognitive and Adaptive Effects of Early Growth Hormone Treatment in Prader-Willi Syndrome Patients: A Cohort StudyAitana Ayet-Roger, Lorena Joga-Elvira, Assumpta Caixàs, et al.
Journal of Clinical Medicine|January 11, 2025
Family Shopping Basket Intervention: A Strategy to Reduce Obesity in Prepubertal ChildrenRocío Escartín, Beatriz de Peray, Yolanda Couto, et al.
The American Journal of Case Reports|June 8, 2017
Gastric Dilatation and Abdominal Compartment Syndrome in a Child with Prader-Willi SyndromeClara Blat, Elisenda Busquets, Teresa Gili, et al.
The American Journal of Case Reports|September 22, 2018
Insulinoma: A Rare Cause of Hypoglycemia in ChildhoodRocío Escartín, Nuria Brun, M Nieves García Monforte, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 13, 2026
Hypercoagulability in Prader-Willi Syndrome: A Case-Control Study Exploring Coagulation Profiles and Thrombotic RiskGriselda Vallès-Cardona, Assumpta Caixàs, Irene Berges, et al.
Journal of Clinical Medicine|June 28, 2023
A Personalized Approach to Determining the Caloric Needs of Children with Prader-Willi Syndrome Treated with Growth HormoneYolanda Couto-Rosende, Diana Garcia-Tirado, Mónica Palacio-Marco, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
BMJ Case Reports|April 6, 2021
Vaginal bleeding in a misdiagnosed Mayer-Rokitansky-Küster-Hauser syndromeMireia Tugues, Bernardo Nuñez, Raquel Corripio
The American Journal of Case Reports|December 19, 2021
A 10-Year-Old Boy with Short Stature and Microcephaly, Diagnosed with Moyamoya Syndrome and Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II)Aurora Eslava, Montserrat Garcia-Puig, Raquel Corripio
BMJ Case Reports|February 2, 2013
Pseudohypoaldosteronism without nephropathy masking salt-wasting congenital adrenal hyperplasia genetically confirmedCarla Balcells, Teresa Gili, Jacobo Pérez, et al.
BMJ Case Reports|July 24, 2013
Disorder of sex development as a diagnostic clue in the first Spanish known newborn with P450 oxidoreductase deficiencyDunia Sánchez-Garvín, Sonia Albaladejo, Begoña Ezquieta, et al.
Journal of Clinical Medicine|March 25, 2022
Cognitive and Adaptive Effects of Early Growth Hormone Treatment in Prader-Willi Syndrome Patients: A Cohort StudyAitana Ayet-Roger, Lorena Joga-Elvira, Assumpta Caixàs, et al.
Journal of Clinical Medicine|January 11, 2025
Family Shopping Basket Intervention: A Strategy to Reduce Obesity in Prepubertal ChildrenRocío Escartín, Beatriz de Peray, Yolanda Couto, et al.
The American Journal of Case Reports|June 8, 2017
Gastric Dilatation and Abdominal Compartment Syndrome in a Child with Prader-Willi SyndromeClara Blat, Elisenda Busquets, Teresa Gili, et al.
The American Journal of Case Reports|September 22, 2018
Insulinoma: A Rare Cause of Hypoglycemia in ChildhoodRocío Escartín, Nuria Brun, M Nieves García Monforte, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 13, 2026
Hypercoagulability in Prader-Willi Syndrome: A Case-Control Study Exploring Coagulation Profiles and Thrombotic RiskGriselda Vallès-Cardona, Assumpta Caixàs, Irene Berges, et al.
Journal of Clinical Medicine|June 28, 2023
A Personalized Approach to Determining the Caloric Needs of Children with Prader-Willi Syndrome Treated with Growth HormoneYolanda Couto-Rosende, Diana Garcia-Tirado, Mónica Palacio-Marco, et al.
Pageof 5