整理番号

論文の種類

著者名

タイトル・題名

雑誌名
書名　外

巻（号）

ページ

年号

Corresponding
Author

1744001

原著

Toda N* Ihara K, Kojima-Ishii K, Ochiai M, Ohkubo K, Kawamoto Y Kohno Y, Kumasaka S, Kawase A, Ueno Y, Futatani T, Miyazawa T, Nagaoki Y, Nakata S, Misaki M, Arai H, Kawai M, Sato M, Yada Y, Takahashi N., Komatsu A, Maki K, Watabe S, Sumida Y, Kuwashima M, Mizumoto H, Sato K, Hara T.

Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann, Sotos and Kabuki syndromes: A nationwide survey in Japan.

Am J Med Genet.

173 (2),

360-367,

2017.

Toda N

1744002

原著

Ihara K*,Fukano, Ayabe T, Fukami M, Ogata T, Kawamura T, Urakami T, Kikuchi N, Yokota I, Takemoto K, Mukai T, Nishii A, Kikuchi T, Mori T, Shimura N, Sasaki G, Kizu R, Takubo N, Soneda S, Fujisawa T, Takaya R, Kizaki Z, Kanzaki S, Hanaki K, Matsuura N, Kasahara Y, Kosaka K, Takahashi T, Minamitani K, Matsuo S, Mochizuki H, Kobayashi K, Koike A, Horikawa R, Teno S, Tsubouchi K, Mochizuki T, Igarashi Y, Amemiya S, Sugihara S, Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes (JSGIT)

FUT2 Nonsecretor Status Links Type 1 Diabetes Susceptibility in Japanese children.

Diabet Med.

34 (4),

586-589,

2017.

Ihara K

1744003

原著

Nagasaka H*,Komatsu H, Inui A, Nakacho M, Morioka I, Tsukahara H, Kaji S, Hirayama S, Miida T, Kondou H, Ihara K, Yagi M, Kizaki Z, Bessho K, Kodama T, Iijima K, Saheki T, Yorifuji T, Honda A.

Circulating tricarboxylic acid cycle metabolite levels in citrin-deficient children with metabolic adaptation, with and without sodium pyruvate treatment.

Mol Genet Metab.

120,

207-212,

2017.

Nagasaka H

1744004

原著

Imagawa E*,Higashimoto K, Sakai Y, Numakura C, Okamoto N, Matsunaga S, Ryo A, Sato Y, Sanefuji M, Ihara K, Takada Y, Nishimura G, Saitsu H, Mizuguchi T, Miyatake S, Nakashima M, Miyake N, Soejima H, Matsumoto N.

Mutations in Genes Encoding Polycomb Repressive Complex 2 Subunits Cause Weaver Syndrome.

Hum Mutat.

38 (6),

637-648,

2017.

Imagawa E

1744005

症例報告

Abe Y*, Matsuduka A, Okanari K, Miyahara H, Kato M, Miyatake S, Saitsu H, Matsumoto N, Tomoki M, Ihara K.

A severe pulmonary complication in a patient with COL4A1-related disorder: A case report.

Eur J Med Genet.

60 (3),

169-171,

2017.

Ihara K

1744006

症例報告

Itonaga T*, Goto H, Toujigamori M, Ohno Y, Korematsu S, Izumi T, Narumi S, Hasegawa T, Ihara K.

Three-quarters adrenalectomy for infantile-onset Cushing syndrome due to bilateral adrenal hyperplasia in McCune-Albright syndrome.

Horm Res Paediatr.

88 (3-4),

285-290,

2017.

Itonaga T

1744007

症例報告

Oba U*, Yamada H, Suenobu SI, Nakamura Y, Ito A, Hatano Y, Itonaga N, Ohshima K, Koga Y, Ohga S, Ihara K.

Toxic epidermal necrolysis in a child 6 months post-hematopoietic stem cell transplantation.

Pediatr Transplant.

21 (5),

e12931,

2017.

Oba U

1744008

原著

Korematsu S*.Yamada H, Miyahara H, Ihara K.

Increased levels of anti-phosphatidylcholine and anti-phosphatidylethanolamine
antibodies in pediatric patients with cerebral infarction.

Brain Dev.

39 (6),

542-546,

2017.

Korematsu S

1744009

原著

Miyahara H*.Yadavilli S, Natsumeda M, Rubens JA, Rodgers L, Kambhampati M, Taylor IC, Kaur H, Asnaghi L, Eberhart CG, Warren KE, Nazarian J, Raabe EH.

The dual mTOR kinase inhibitor TAK228 inhibits tumorigenicity and enhances
radiosensitization in diffuse intrinsic pontine glioma.

Cancer Lett.

400,

110-116,

2017.

Raabe EH

1744010

原著

Kato R*.Miyahara H, Kawano T, Matsuzuka A, Noda K, Izumi T.

Heparan sulfate storage in the cardiac conduction system triggers
atrioventricular block.

Brain Dev.

39 (5),

418-421,

2017.

Izumi T

1744011

原著

Sato-Kawano N*.Takemoto M, Okabe E, Yokote K, Matsuo M, Kosaki R, Ihara K.

The clinical characteristics of Asian patients with classical-type Hutchinson-Gilford progeria syndrome.

J Hum Genet.

62 (12),

1031-1035,

2017.

Ihara K

1744012

症例報告

Kawano F*.Itonaga T, Inoue M, Maeda M, Miyahara H, Ihara K.

Central hypoadrenocorticism associated with Rathke's cleft cyst.

Neuroendocrinology Letters.

38 (3),

141-144,

2017.

Ihara K

1744013

症例報告

Goto H*.Kimura M, Hirano N, Suenobu S, Ihara K.

NUP98-HOXC13 fusion gene in acute myeloid leukemia: Pediatric case.

Pediatr Int.

59 (10),

1105-1106,

2017.

Goto H

1744014

著書

井原健二

Leigh脳症、Reye症候群.

内科学.
矢崎義雄総編集,　朝倉書院,　東京

第11版,

2217-2218,

2017.

井原健二

1744015

症例報告

後藤洋徳*.中嶋美咲, 宮原弘明, 末延聡一, 宗内淳, 落合由恵, 笹栗毅和, 井原健二.

臨床研究・症例報告経時的な画像検査により適切な手術範囲と時期を検討し得たPHACE症候群の1例.

小児科臨床.　

70 (8),

1289-1293,

2017.

後藤洋徳

1744016

総説

末延聡一

リンパ節腫大（特集　日常生活にひそむ小児血液・腫瘍性疾患）.

小児科診療.

80 (10),

1253-1260,

2017.

末延聡一

1744017

症例報告

Kawasaki Y*.Uchida S, Onishi K, Toyokuni M, Okanari K, Fujiki M

Intraoperative Neurophysiologic Monitoring for Prediction of Postoperative Neurological Improvement in a Child With Chiari Type I Malformation.

J Craniofac Surg.

28 (7),

1837-1841,

2017.

Kawasaki Y

1744018

原著

Okanari K*.Otsubo H, Kouzmitcheva E, Rangrej J, Baba S, Ochi A, Okanishi T, Homma Y, Nita DA, Donner EJ

Ictal Symmetric Tonic Extension Posturing and Postictal Generalized EEG Suppression Arising From Sleep in Children With Epilepsy.

Pediatr Neurol.

76,

54-59,

2017.

Donner EJ

小児科学
Pediatrics
整理番号	論文の種類	著者名	タイトル・題名	雑誌名書名　外	巻（号）	ページ	年号	Corresponding Author
1744001	原著	Toda N* Ihara K, Kojima-Ishii K, Ochiai M, Ohkubo K, Kawamoto Y Kohno Y, Kumasaka S, Kawase A, Ueno Y, Futatani T, Miyazawa T, Nagaoki Y, Nakata S, Misaki M, Arai H, Kawai M, Sato M, Yada Y, Takahashi N., Komatsu A, Maki K, Watabe S, Sumida Y, Kuwashima M, Mizumoto H, Sato K, Hara T.	Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann, Sotos and Kabuki syndromes: A nationwide survey in Japan.	Am J Med Genet.	173 (2),	360-367,	2017.	Toda N
1744002	原著	Ihara K*,Fukano, Ayabe T, Fukami M, Ogata T, Kawamura T, Urakami T, Kikuchi N, Yokota I, Takemoto K, Mukai T, Nishii A, Kikuchi T, Mori T, Shimura N, Sasaki G, Kizu R, Takubo N, Soneda S, Fujisawa T, Takaya R, Kizaki Z, Kanzaki S, Hanaki K, Matsuura N, Kasahara Y, Kosaka K, Takahashi T, Minamitani K, Matsuo S, Mochizuki H, Kobayashi K, Koike A, Horikawa R, Teno S, Tsubouchi K, Mochizuki T, Igarashi Y, Amemiya S, Sugihara S, Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes (JSGIT)	FUT2 Nonsecretor Status Links Type 1 Diabetes Susceptibility in Japanese children.	Diabet Med.	34 (4),	586-589,	2017.	Ihara K
1744003	原著	Nagasaka H*,Komatsu H, Inui A, Nakacho M, Morioka I, Tsukahara H, Kaji S, Hirayama S, Miida T, Kondou H, Ihara K, Yagi M, Kizaki Z, Bessho K, Kodama T, Iijima K, Saheki T, Yorifuji T, Honda A.	Circulating tricarboxylic acid cycle metabolite levels in citrin-deficient children with metabolic adaptation, with and without sodium pyruvate treatment.	Mol Genet Metab.	120,	207-212,	2017.	Nagasaka H
1744004	原著	Imagawa E*,Higashimoto K, Sakai Y, Numakura C, Okamoto N, Matsunaga S, Ryo A, Sato Y, Sanefuji M, Ihara K, Takada Y, Nishimura G, Saitsu H, Mizuguchi T, Miyatake S, Nakashima M, Miyake N, Soejima H, Matsumoto N.	Mutations in Genes Encoding Polycomb Repressive Complex 2 Subunits Cause Weaver Syndrome.	Hum Mutat.	38 (6),	637-648,	2017.	Imagawa E
1744005	症例報告	Abe Y*, Matsuduka A, Okanari K, Miyahara H, Kato M, Miyatake S, Saitsu H, Matsumoto N, Tomoki M, Ihara K.	A severe pulmonary complication in a patient with COL4A1-related disorder: A case report.	Eur J Med Genet.	60 (3),	169-171,	2017.	Ihara K
1744006	症例報告	Itonaga T*, Goto H, Toujigamori M, Ohno Y, Korematsu S, Izumi T, Narumi S, Hasegawa T, Ihara K.	Three-quarters adrenalectomy for infantile-onset Cushing syndrome due to bilateral adrenal hyperplasia in McCune-Albright syndrome.	Horm Res Paediatr.	88 (3-4),	285-290,	2017.	Itonaga T
1744007	症例報告	Oba U*, Yamada H, Suenobu SI, Nakamura Y, Ito A, Hatano Y, Itonaga N, Ohshima K, Koga Y, Ohga S, Ihara K.	Toxic epidermal necrolysis in a child 6 months post-hematopoietic stem cell transplantation.	Pediatr Transplant.	21 (5),	e12931,	2017.	Oba U
1744008	原著	Korematsu S*.Yamada H, Miyahara H, Ihara K.	Increased levels of anti-phosphatidylcholine and anti-phosphatidylethanolamine antibodies in pediatric patients with cerebral infarction.	Brain Dev.	39 (6),	542-546,	2017.	Korematsu S
1744009	原著	Miyahara H*.Yadavilli S, Natsumeda M, Rubens JA, Rodgers L, Kambhampati M, Taylor IC, Kaur H, Asnaghi L, Eberhart CG, Warren KE, Nazarian J, Raabe EH.	The dual mTOR kinase inhibitor TAK228 inhibits tumorigenicity and enhances radiosensitization in diffuse intrinsic pontine glioma.	Cancer Lett.	400,	110-116,	2017.	Raabe EH
1744010	原著	Kato R*.Miyahara H, Kawano T, Matsuzuka A, Noda K, Izumi T.	Heparan sulfate storage in the cardiac conduction system triggers atrioventricular block.	Brain Dev.	39 (5),	418-421,	2017.	Izumi T
1744011	原著	Sato-Kawano N*.Takemoto M, Okabe E, Yokote K, Matsuo M, Kosaki R, Ihara K.	The clinical characteristics of Asian patients with classical-type Hutchinson-Gilford progeria syndrome.	J Hum Genet.	62 (12),	1031-1035,	2017.	Ihara K
1744012	症例報告	Kawano F*.Itonaga T, Inoue M, Maeda M, Miyahara H, Ihara K.	Central hypoadrenocorticism associated with Rathke's cleft cyst.	Neuroendocrinology Letters.	38 (3),	141-144,	2017.	Ihara K
1744013	症例報告	Goto H*.Kimura M, Hirano N, Suenobu S, Ihara K.	NUP98-HOXC13 fusion gene in acute myeloid leukemia: Pediatric case.	Pediatr Int.	59 (10),	1105-1106,	2017.	Goto H
1744014	著書	井原健二	Leigh脳症、Reye症候群.	内科学. 矢崎義雄総編集,　朝倉書院,　東京	第11版,	2217-2218,	2017.	井原健二
1744015	症例報告	後藤洋徳*.中嶋美咲, 宮原弘明, 末延聡一, 宗内淳, 落合由恵, 笹栗毅和, 井原健二.	臨床研究・症例報告経時的な画像検査により適切な手術範囲と時期を検討し得たPHACE症候群の1例.	小児科臨床.	70 (8),	1289-1293,	2017.	後藤洋徳
1744016	総説	末延聡一	リンパ節腫大（特集　日常生活にひそむ小児血液・腫瘍性疾患）.	小児科診療.	80 (10),	1253-1260,	2017.	末延聡一
1744017	症例報告	Kawasaki Y*.Uchida S, Onishi K, Toyokuni M, Okanari K, Fujiki M	Intraoperative Neurophysiologic Monitoring for Prediction of Postoperative Neurological Improvement in a Child With Chiari Type I Malformation.	J Craniofac Surg.	28 (7),	1837-1841,	2017.	Kawasaki Y
1744018	原著	Okanari K*.Otsubo H, Kouzmitcheva E, Rangrej J, Baba S, Ochi A, Okanishi T, Homma Y, Nita DA, Donner EJ	Ictal Symmetric Tonic Extension Posturing and Postictal Generalized EEG Suppression Arising From Sleep in Children With Epilepsy.	Pediatr Neurol.	76,	54-59,	2017.	Donner EJ