整理番号

論文の種類

著者名

タイトル

雑誌名
書名　外

巻（号）

ページ

年号

Correspo
nding
Author

1644001

原著

Korematsu S, Takano T, Izumi T.

Pre-school development and behavior screening with a consecutive support programs for 5-year-olds reduces the rate of school refusal.

Brain Dev

38 (4).

373－376.

2016.

Korematsu S.

1644002

総説

是松聖悟.

感染症と気管支喘息－過去、現在、そしてエンテロウイルスD68の流行から未来への展望－

臨床とウイルス

44 (3)

95-100

2016.

是松聖悟.

1644003

総説

是松聖悟,山内秀雄.

「MRI検査時の鎮静に関する共同提言」からの発展と課題

脳と発達

48 (2)

107-110

2016.

是松聖悟.

1644004

原著

Toda N*, Hoshina T, Koga Y, Ochiai M, Kaku N, Yamamura K, Torisu H, Ihara K, Takada H, Maehara Y, Hara T.

Analysis of the death due to infectious diseases in the patients hospitalized in the pediatric ward of a single Japanese tertiary medical facility.

Jpn J Infect Dis

69(6)

464-470

2016.

Hoshina T

1644005

原著

Fukai R*, Saitsu H, Okamoto N, Sakai Y, Fattal-Valevski A, Masaaki S, Kitai Y, Torio M, Kojima-Ishii K, Ihara K, Chernuha V, Nakashima M, Miyatake S, Tanaka F, Miyake N, Matsumoto N.

De novo missense mutations in NALCN cause developmental and intellectual impairment with hypotonia.

J Hum Genet

61(5)

451-455

2016.

Matsumoto N

1644006

原著

Narumi S*, Amano N, Ishii T, Katsumata N, Muroya K, Adachi M, Toyoshima K, Tanaka Y, Fukuzawa R, Miyako K, Kinjo S, Ohga S, Ihara K, Inoue H, Kinjo T, Hara T, Kohno M, Yamada S, Urano H, Kitagawa Y, Tsugawa K, Higa A, Miyawaki M, Okutani T, Kizaki Z,Hamada.H, Kihara M, Shiga K, Yamaguchi T, Kenmochi M, Kitajima H, Fukami M, Shimizu A, Kudoh J, Shibata S, Okano H, Miyake N, Matsumoto N, Hasegawa T.

SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7.

Nat Genet

48(7)

792-797

2016.

Hasegawa T

1644007

原著

Ishii T*, Fukuzawa R, Sato T, Muroya K, Adachi M, Ihara K, Igaki J, Hasegawa Y, Sato S, Mitsui T, Hasegawa T.

Gonadal macrophage infiltration in congenital lipoid adrenal hyperplasia.

Eur J Endocrinol

175(2)

127-32

2016.

Ishii T

1644008

症例報告

Nagata H*, Yamamura K, Nagata K, Uike K, Morihana E, Ihara K, Yumoto Y, Fusazaki N, Kado H, Kato K, Taguchi T, Hara T.

Management of congenital diaphragmatic hernia with transposition of the great arteries.

Pediatr Int

58(6)

516-518

2016.

Nagata H

1644009

症例報告

Kuga S*, Goto H, Okanari K, Maeda T, Ihara K.

Reversible cerebral vasoconstriction syndrome manifesting as focal seizures without a thunderclap headache: A pediatric case report.

Brain Dev

38(9)

880-883

2016.

Kuga S

1644010

症例報告

Akiyoshi K*, Sekiguchi K, Okamoto T, Suenobu S, Izumi T.

Cord blood transplantation in a young child with pyruvate kinase deficiency.

Pediatr Int.

58

634-6

2016.

Akiyoshi K

1644011

総説

吉村淳一, 宮原弘明、棗田　学、柿田明美、藤井幸彦.

髄芽腫の予後因子Gli3

日本臨床増刊号　脳腫瘍学

74

292-297

2016.

吉村淳一

1644012

原著

Natsumeda M*, Maitani K, Liu Y, Miyahara H, Kaur H, Chu Q, Zhang H, Kahlert UD, Eberhart CG.

Targeting Notch Signaling and Autophagy Increases Cytotoxicity in Glioblastoma
Neurospheres.

Brain Pathol.

26(6)

713-723.

2016.

Eberhart CG

1644013

原著

Maeda T*, Inoue M, Sekiguchi K, Ihara K.

Aminophylline-associated irritable behaviour in preterm neonates

Ear Hum Dev.

99

37-41

2016.

Maeda T

1644014

原著

Koga H*, Iida K, Maeda T, Takahashi M, Fukushima N, Goshi T.

Epidemiologic research on malformations associated with cleft lip and cleft palate in Japan

Plos Onw

22

11e0149773

2016.

Koga H

1644015

症例報告

Ono M*, Maeda T, Ihara K.

The first mixoploidy infant with full triploidy in blood cells.

Pediatr Int

58

1354-5

2016.

Ono M

1644016

原著

Ayabe T*, Fukami M, Ogata T, Kawamura T, Urakami T, Kikuchi N, Yokota I, Ihara K, 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):

Variants associated with autoimmune Type 1 diabetes in Japanese children: implications for age-specific effects of cis-regulatory haplotypes at 17q12-q21.

Diabet Med

33(12)

1717-1722

2016.

Fukami M

1644017

原著

Ochiai M*, Matsushita Y, Inoue H, Kusuda T, Kang D, Ichihara K, Nakashima N, Ihara K, Ohga S, Hara T.

Blood Reference Intervals for Preterm Low-Birth-Weight Infants: A Multicenter Cohort Study in Japan.

PLoS One

11(8)

e0161439

2016.

Ochiai M

1644018

著書

井原健二.

先天性甲状腺機能低下症

今日の治療指針2016年版

1446-1447

2016.

1644019

原著

Imamura T*, Yano M, Asai D, Moriya-Saito A, Suenobu SI, Hasegawa D, Deguchi T, Hashii Y, Kawasaki H, Hori H, Yumura-Yagi K, Hara J, Horibe K, Sato A.

IKZF1 deletion is enriched in pediatric B-cell precursor acute lymphoblastic leukemia patients showing prednisolone resistance.

Leukemia

30

1801-1803

2016.

Imamura T

小児科学
Pediatrics
整理番号	論文の種類	著者名	タイトル	雑誌名書名　外	巻（号）	ページ	年号	Correspo nding Author
1644001	原著	Korematsu S, Takano T, Izumi T.	Pre-school development and behavior screening with a consecutive support programs for 5-year-olds reduces the rate of school refusal.	Brain Dev	38 (4).	373－376.	2016.	Korematsu S.
1644002	総説	是松聖悟.	感染症と気管支喘息－過去、現在、そしてエンテロウイルスD68の流行から未来への展望－	臨床とウイルス	44 (3)	95-100	2016.	是松聖悟.
1644003	総説	是松聖悟,山内秀雄.	「MRI検査時の鎮静に関する共同提言」からの発展と課題	脳と発達	48 (2)	107-110	2016.	是松聖悟.
1644004	原著	Toda N*, Hoshina T, Koga Y, Ochiai M, Kaku N, Yamamura K, Torisu H, Ihara K, Takada H, Maehara Y, Hara T.	Analysis of the death due to infectious diseases in the patients hospitalized in the pediatric ward of a single Japanese tertiary medical facility.	Jpn J Infect Dis	69(6)	464-470	2016.	Hoshina T
1644005	原著	Fukai R*, Saitsu H, Okamoto N, Sakai Y, Fattal-Valevski A, Masaaki S, Kitai Y, Torio M, Kojima-Ishii K, Ihara K, Chernuha V, Nakashima M, Miyatake S, Tanaka F, Miyake N, Matsumoto N.	De novo missense mutations in NALCN cause developmental and intellectual impairment with hypotonia.	J Hum Genet	61(5)	451-455	2016.	Matsumoto N
1644006	原著	Narumi S*, Amano N, Ishii T, Katsumata N, Muroya K, Adachi M, Toyoshima K, Tanaka Y, Fukuzawa R, Miyako K, Kinjo S, Ohga S, Ihara K, Inoue H, Kinjo T, Hara T, Kohno M, Yamada S, Urano H, Kitagawa Y, Tsugawa K, Higa A, Miyawaki M, Okutani T, Kizaki Z,Hamada.H, Kihara M, Shiga K, Yamaguchi T, Kenmochi M, Kitajima H, Fukami M, Shimizu A, Kudoh J, Shibata S, Okano H, Miyake N, Matsumoto N, Hasegawa T.	SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7.	Nat Genet	48(7)	792-797	2016.	Hasegawa T
1644007	原著	Ishii T*, Fukuzawa R, Sato T, Muroya K, Adachi M, Ihara K, Igaki J, Hasegawa Y, Sato S, Mitsui T, Hasegawa T.	Gonadal macrophage infiltration in congenital lipoid adrenal hyperplasia.	Eur J Endocrinol	175(2)	127-32	2016.	Ishii T
1644008	症例報告	Nagata H*, Yamamura K, Nagata K, Uike K, Morihana E, Ihara K, Yumoto Y, Fusazaki N, Kado H, Kato K, Taguchi T, Hara T.	Management of congenital diaphragmatic hernia with transposition of the great arteries.	Pediatr Int	58(6)	516-518	2016.	Nagata H
1644009	症例報告	Kuga S*, Goto H, Okanari K, Maeda T, Ihara K.	Reversible cerebral vasoconstriction syndrome manifesting as focal seizures without a thunderclap headache: A pediatric case report.	Brain Dev	38(9)	880-883	2016.	Kuga S
1644010	症例報告	Akiyoshi K*, Sekiguchi K, Okamoto T, Suenobu S, Izumi T.	Cord blood transplantation in a young child with pyruvate kinase deficiency.	Pediatr Int.	58	634-6	2016.	Akiyoshi K
1644011	総説	吉村淳一, 宮原弘明、棗田　学、柿田明美、藤井幸彦.	髄芽腫の予後因子Gli3	日本臨床増刊号　脳腫瘍学	74	292-297	2016.	吉村淳一
1644012	原著	Natsumeda M*, Maitani K, Liu Y, Miyahara H, Kaur H, Chu Q, Zhang H, Kahlert UD, Eberhart CG.	Targeting Notch Signaling and Autophagy Increases Cytotoxicity in Glioblastoma Neurospheres.	Brain Pathol.	26(6)	713-723.	2016.	Eberhart CG
1644013	原著	Maeda T*, Inoue M, Sekiguchi K, Ihara K.	Aminophylline-associated irritable behaviour in preterm neonates	Ear Hum Dev.	99	37-41	2016.	Maeda T
1644014	原著	Koga H*, Iida K, Maeda T, Takahashi M, Fukushima N, Goshi T.	Epidemiologic research on malformations associated with cleft lip and cleft palate in Japan	Plos Onw	22	11e0149773	2016.	Koga H
1644015	症例報告	Ono M*, Maeda T, Ihara K.	The first mixoploidy infant with full triploidy in blood cells.	Pediatr Int	58	1354-5	2016.	Ono M
1644016	原著	Ayabe T*, Fukami M, Ogata T, Kawamura T, Urakami T, Kikuchi N, Yokota I, Ihara K, 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):	Variants associated with autoimmune Type 1 diabetes in Japanese children: implications for age-specific effects of cis-regulatory haplotypes at 17q12-q21.	Diabet Med	33(12)	1717-1722	2016.	Fukami M
1644017	原著	Ochiai M*, Matsushita Y, Inoue H, Kusuda T, Kang D, Ichihara K, Nakashima N, Ihara K, Ohga S, Hara T.	Blood Reference Intervals for Preterm Low-Birth-Weight Infants: A Multicenter Cohort Study in Japan.	PLoS One	11(8)	e0161439	2016.	Ochiai M
1644018	著書	井原健二.	先天性甲状腺機能低下症	今日の治療指針2016年版		1446-1447	2016.
1644019	原著	Imamura T*, Yano M, Asai D, Moriya-Saito A, Suenobu SI, Hasegawa D, Deguchi T, Hashii Y, Kawasaki H, Hori H, Yumura-Yagi K, Hara J, Horibe K, Sato A.	IKZF1 deletion is enriched in pediatric B-cell precursor acute lymphoblastic leukemia patients showing prednisolone resistance.	Leukemia	30	1801-1803	2016.	Imamura T