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Yumi Asakura

Showing results (1-10 of 64) with videos related to

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Cranio : the Journal of Craniomandibular Practice|September 26, 2014
Myhre syndrome: a rare craniofacial disorderNaho Ishibashi, Yasunori Sasaki, Yumi Asakura
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|March 6, 2009
Unfavorable lipoprotein profile in childhood cancer survivors with suprasellar brain tumors--a high Apo B level and increased small dense LDL-cholesterolMasanori Adachi, Koji Muroya, Yumi Asakura
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 29, 2010
Growth hormone response to GH-releasing peptide-2 in childrenYumi Asakura, Yuko Toyota, Koji Muroya, et al.
Journal of Medical Case Reports|January 1, 2014
Classic Bartter syndrome complicated with profound growth hormone deficiency: a case reportMasanori Adachi, Toshihiro Tajima, Koji Muroya, et al.
Acta Paediatrica (Oslo, Norway : 1992)|November 24, 2005
Usefulness of pancreatic ultrasonography in the diagnosis of Shwachman-Bodian-Diamond syndromeMasanori Adachi, Katsuhiko Tachibana, Yumi Asakura, et al.
Endocrine Journal|November 24, 2020
Metreleptin worked in a diabetic woman with a history of hematopoietic stem cell transplantation (HSCT) during infancy: further support for the concept of 'HSCT-associated lipodystrophy'Masanori Adachi, Koji Muroya, Junko Hanakawa, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 20, 2004
Abnormal steroidogenesis in three patients with Antley-Bixler syndrome: apparent decreased activity of 17alpha-hydroxylase, 17,20-lyase and 21-hydroxylaseMasanori Adachi, Yumi Asakura, Katsuhiko Tachibana, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 3, 2006
A novel mutation in the GATA3 gene in a family with HDR syndrome (Hypoparathyroidism, sensorineural Deafness and Renal anomaly syndrome)Masanori Adachi, Katsuhiko Tachibana, Yumi Asakura, et al.
The Journal of Clinical Endocrinology and Metabolism|September 9, 2011
Molecular basis of thyroid dyshormonogenesis: genetic screening in population-based Japanese patientsSatoshi Narumi, Koji Muroya, Yumi Asakura, et al.
Thyroid Research|July 10, 2015
The ratio of serum free triiodothyronine to free thyroxine in children: a retrospective database survey of healthy short individuals and patients with severe thyroid hypoplasia or central hypothyroidismYuji Oto, Koji Muroya, Junko Hanakawa, et al.
Pageof 7

Showing results (1-10 of 64) with videos related to

Sort By:
Pageof 7
Cranio : the Journal of Craniomandibular Practice|September 26, 2014
Myhre syndrome: a rare craniofacial disorderNaho Ishibashi, Yasunori Sasaki, Yumi Asakura
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|March 6, 2009
Unfavorable lipoprotein profile in childhood cancer survivors with suprasellar brain tumors--a high Apo B level and increased small dense LDL-cholesterolMasanori Adachi, Koji Muroya, Yumi Asakura
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 29, 2010
Growth hormone response to GH-releasing peptide-2 in childrenYumi Asakura, Yuko Toyota, Koji Muroya, et al.
Journal of Medical Case Reports|January 1, 2014
Classic Bartter syndrome complicated with profound growth hormone deficiency: a case reportMasanori Adachi, Toshihiro Tajima, Koji Muroya, et al.
Acta Paediatrica (Oslo, Norway : 1992)|November 24, 2005
Usefulness of pancreatic ultrasonography in the diagnosis of Shwachman-Bodian-Diamond syndromeMasanori Adachi, Katsuhiko Tachibana, Yumi Asakura, et al.
Endocrine Journal|November 24, 2020
Metreleptin worked in a diabetic woman with a history of hematopoietic stem cell transplantation (HSCT) during infancy: further support for the concept of 'HSCT-associated lipodystrophy'Masanori Adachi, Koji Muroya, Junko Hanakawa, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 20, 2004
Abnormal steroidogenesis in three patients with Antley-Bixler syndrome: apparent decreased activity of 17alpha-hydroxylase, 17,20-lyase and 21-hydroxylaseMasanori Adachi, Yumi Asakura, Katsuhiko Tachibana, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 3, 2006
A novel mutation in the GATA3 gene in a family with HDR syndrome (Hypoparathyroidism, sensorineural Deafness and Renal anomaly syndrome)Masanori Adachi, Katsuhiko Tachibana, Yumi Asakura, et al.
The Journal of Clinical Endocrinology and Metabolism|September 9, 2011
Molecular basis of thyroid dyshormonogenesis: genetic screening in population-based Japanese patientsSatoshi Narumi, Koji Muroya, Yumi Asakura, et al.
Thyroid Research|July 10, 2015
The ratio of serum free triiodothyronine to free thyroxine in children: a retrospective database survey of healthy short individuals and patients with severe thyroid hypoplasia or central hypothyroidismYuji Oto, Koji Muroya, Junko Hanakawa, et al.
Pageof 7