Interstitial Lung Disease in Childhood: Clinical and Genetic Aspects

Yazar: Kitazawa, Hiroshi, Kure, Shigeo
Yayımlandı Clin Med Insights Circ Respir Pulm Med (2015)

Visualization of Thrombosis on a Prosthetic Pulmonary Valve Using Electrocardiogram-Gated Multidetector Computed Tomography

Yazar: Kakizaki, Shuhei, Tazawa, Seiichi, Kure, Shigeo, Saiki, Yoshikatsu
Yayımlandı Thorac Cardiovasc Surg Rep (2014)

Successful Treatment of an Infant with Left Ventricular Noncompaction Presenting with Fatal Ventricular Arrhythmia Treated with Cardiac Resynchronization Therapy and an Implantable...

Yazar: Kimura, Masato, Kawano, Kengo, Yaoita, Hisao, Kure, Shigeo
Yayımlandı Case Rep Cardiol (2018)

Asymptomatic left atrial appendage aneurysm (LAAA) with pericardial defect in a 1-year-old girl

Yazar: Ota, Chiharu, Kimura, Masato, Kitami, Masahiro, Kure, Shigeo
Yayımlandı BMJ Case Rep (2018)

Neurofibromatosis Type 1 Complicated by Atypical Coarctation of the Thoracic Aorta

Yazar: Kimura, Masato, Kakizaki, Shuhei, Kawano, Kengo, Sato, Shinichi, Kure, Shigeo
Baskı/Yayın Bilgisi 2013

Nateglinide is Effective for Diabetes Mellitus with Reactive Hypoglycemia in a Child with a Compound Heterozygous ABCC8 Mutation

Yazar: Saito-Hakoda, Akiko, Yorifuji, Tohru, Kanno, Junko, Kure, Shigeo, Fujiwara, Ikuma
Baskı/Yayın Bilgisi 2012

Hypoketotic hypoglycemia in citrin deficiency: a case report

Yazar: Wada, Yoichi, Arai-Ichinoi, Natsuko, Kikuchi, Atsuo, Sakamoto, Osamu, Kure, Shigeo
Yayımlandı BMC Pediatr (2020)

Postpartum Deterioration of Hemodynamics in a Case of Uncorrected Ebstein's Anomaly

Yazar: Kimura, Masato, Kakizaki, Shuhei, Tazawa, Seiichi, Adachi, Osamu, Saiki, Yoshikatsu, Kure, Shigeo
Baskı/Yayın Bilgisi 2012

Central Venous Catheter-Related Bloodstream Infection with Kocuria kristinae in a Patient with Propionic Acidemia

Yazar: Kimura, Masato, Kawai, Eichiro, Yaoita, Hisao, Ichinoi, Natsuko, Sakamoto, Osamu, Kure, Shigeo
Yayımlandı Case Rep Infect Dis (2017)

Genomic deletion within GLDC is a major cause of non‐ketotic hyperglycinaemia

Yazar: Kanno, Junko, Hutchin, Tim, Kamada, Fumiaki, Narisawa, Ayumi, Aoki, Yoko, Matsubara, Yoichi, Kure, Shigeo
Baskı/Yayın Bilgisi 2007

Screening of SLC25A13 mutation in the Thai population

Yazar: Wongkittichote, Parith, Sukasem, Chonlaphat, Kikuchi, Atsuo, Aekplakorn, Wichai, Jensen, Laran T, Kure, Shigeo, Wattanasirichaigoon, Duangrurdee
Baskı/Yayın Bilgisi 2013

Genetics and Biomarkers of Moyamoya Disease: Significance of RNF213 as a Susceptibility Gene

Yazar: Fujimura, Miki, Sonobe, Shinya, Nishijima, Yasuo, Niizuma, Kuniyasu, Sakata, Hiroyuki, Kure, Shigeo, Tominaga, Teiji
Baskı/Yayın Bilgisi 2014

Phenytoin-responsive epileptic encephalopathy with a tandem duplication involving FGF12

Yazar: Shi, Rui-Ming, Kobayashi, Tomoko, Kikuchi, Atsuo, Sato, Ryo, Uematsu, Mitsugu, An, Kumiko, Kure, Shigeo
Yayımlandı Neurol Genet (2017)

Evolution into moyamoya disease in an infant with internal carotid artery aneurysms

Yazar: Tanaka, Ryosuke, Takahashi, Satoru, Okano, Satomi, Okayama, Akie, Suzuki, Nao, Kure, Shigeo, Azuma, Hiroshi
Yayımlandı eNeurologicalSci (2017)

The effect of dietary protein restriction in a case of molybdenum cofactor deficiency with MOCS1 mutation

Yazar: Abe, Yu, Aihara, Yu, Endo, Wakaba, Hasegawa, Hiroshi, Ichida, Kimiyoshi, Uematsu, Mitsugu, Kure, Shigeo
Yayımlandı Mol Genet Metab Rep (2021)

Small Maf Compound Mutants Display Central Nervous System Neuronal Degeneration, Aberrant Transcription, and Bach Protein Mislocalization Coincident with Myoclonus and Abnormal Sta...

Yazar: Katsuoka, Fumiki, Motohashi, Hozumi, Tamagawa, Yuna, Kure, Shigeo, Igarashi, Kazuhiko, Engel, James Douglas, Yamamoto, Masayuki
Baskı/Yayın Bilgisi 2003

Depletion of Molecular Chaperones from the Endoplasmic Reticulum and Fragmentation of the Golgi Apparatus Associated with Pathogenesis in Pelizaeus-Merzbacher Disease

Yazar: Numata, Yurika, Morimura, Toshifumi, Nakamura, Shoko, Hirano, Eriko, Kure, Shigeo, Goto, Yu-ich, Inoue, Ken
Baskı/Yayın Bilgisi 2013

Brain White Matter Abnormality in a Newborn Infant with Congenital Adrenal Hyperplasia

Yazar: Kaga, Akimune, Saito-hakoda, Akiko, Uematsu, Mitsugu, Kamimura, Miki, Kanno, Junko, Kure, Shigeo, Fujiwara, Ikuma
Baskı/Yayın Bilgisi 2013

A follow-up during puberty in a Japanese girl with type A insulin resistance due to a novel mutation in INSR

Yazar: Saito-Hakoda, Akiko, Nishii, Aki, Uchida, Takashi, Kikuchi, Atsuo, Kanno, Junko, Fujiwara, Ikuma, Kure, Shigeo
Yayımlandı Clin Pediatr Endocrinol (2018)

Development of icterus gravis in a preterm infant with G71R UGT1A1 polymorphism

Yazar: Kaga, Akimune, Ohkubo, Yukimune, Watanabe, Yohei, Saito, Sachiko, Matsuki, Takuma, Usuda, Haruo, Kanda, Susumu, Suzuki, Yutaka, Tanabu, Muneyuki, Kure, Shigeo
Baskı/Yayın Bilgisi 2013