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Dinesh Giri

Showing results (31-40 of 43) with videos related to

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Drug Delivery|June 18, 2014
Novel flavonoid-based biodegradable nanoparticles for effective oral delivery of etoposide by P-glycoprotein modulation: an in vitro, ex vivo and in vivo investigationsSharmeen Fatma, Sushama Talegaonkar, Zeenat Iqbal, et al.
Journal of Clinical Research in Pediatric Endocrinology|September 20, 2021
Qualitative Parental Perceptions of a Paediatric Multidisciplinary Team Clinic for Prader-Willi SyndromeJennifer S. Cox, Claire Semple, Rhian Augustus, et al.
Case Reports in Genetics|November 13, 2018
A Rare Case of Heterozygous Gain of Function Thyrotropin Receptor Mutation Associated with Development of Thyroid Follicular CarcinomaJames Blackburn, Dinesh Giri, Barbara Ciolka, et al.
World Journal of Oncology|November 18, 2017
Denosumab Therapy for Refractory Hypercalcemia Secondary to Squamous Cell Carcinoma of Skin in Epidermolysis BullosaDinesh Giri, Renuka Ramakrishnan, James Hayden, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 25, 2023
Rapid-onset obesity, hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome - neuro-endocrine tumours (ROHHAD-NET): case series and learning pointsKatherine Hawton, Tom Hilliard, Simon C Langton-Hewer, et al.
BMJ Open|July 23, 2024
Insights from the ACTION Teens Study: a survey of adolescents living with obesity, their caregivers and healthcare professionals in the UKJason C G Halford, Adrian Brown, Kenneth Clare, et al.
Human Molecular Genetics|October 4, 2017
Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalitiesDinesh Giri, Maria Lillina Vignola, Angelica Gualtieri, et al.
Hormone Research in Paediatrics|June 8, 2020
Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB MutationsDinesh Giri, Detlef Bockenhauer, Charu Deshpande, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 26, 2022
Rituximab therapy in ROHHAD(NET) syndromeKatherine A C Hawton, Rainer Doffinger, Athimalaipet V Ramanan, et al.
American Journal of Medical Genetics. Part A|August 13, 2020
Expanding the phenotypic spectrum of IFT81: Associated ciliopathy syndromeTazeen Ashraf, Camelia Vaina, Dinesh Giri, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Drug Delivery|June 18, 2014
Novel flavonoid-based biodegradable nanoparticles for effective oral delivery of etoposide by P-glycoprotein modulation: an in vitro, ex vivo and in vivo investigationsSharmeen Fatma, Sushama Talegaonkar, Zeenat Iqbal, et al.
Journal of Clinical Research in Pediatric Endocrinology|September 20, 2021
Qualitative Parental Perceptions of a Paediatric Multidisciplinary Team Clinic for Prader-Willi SyndromeJennifer S. Cox, Claire Semple, Rhian Augustus, et al.
Case Reports in Genetics|November 13, 2018
A Rare Case of Heterozygous Gain of Function Thyrotropin Receptor Mutation Associated with Development of Thyroid Follicular CarcinomaJames Blackburn, Dinesh Giri, Barbara Ciolka, et al.
World Journal of Oncology|November 18, 2017
Denosumab Therapy for Refractory Hypercalcemia Secondary to Squamous Cell Carcinoma of Skin in Epidermolysis BullosaDinesh Giri, Renuka Ramakrishnan, James Hayden, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 25, 2023
Rapid-onset obesity, hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome - neuro-endocrine tumours (ROHHAD-NET): case series and learning pointsKatherine Hawton, Tom Hilliard, Simon C Langton-Hewer, et al.
BMJ Open|July 23, 2024
Insights from the ACTION Teens Study: a survey of adolescents living with obesity, their caregivers and healthcare professionals in the UKJason C G Halford, Adrian Brown, Kenneth Clare, et al.
Human Molecular Genetics|October 4, 2017
Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalitiesDinesh Giri, Maria Lillina Vignola, Angelica Gualtieri, et al.
Hormone Research in Paediatrics|June 8, 2020
Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB MutationsDinesh Giri, Detlef Bockenhauer, Charu Deshpande, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 26, 2022
Rituximab therapy in ROHHAD(NET) syndromeKatherine A C Hawton, Rainer Doffinger, Athimalaipet V Ramanan, et al.
American Journal of Medical Genetics. Part A|August 13, 2020
Expanding the phenotypic spectrum of IFT81: Associated ciliopathy syndromeTazeen Ashraf, Camelia Vaina, Dinesh Giri, et al.
Pageof 5