Publications by authors named "Mahoko Furujo"

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Seven-year-old boy with severe dyspnoea and influenza virus infection.
Shintaro Fujiwara, Yousuke Higuchi, Mahoko Furujo, Mayu Goda, Yuki Takigawa

J Paediatr Child Health· October 2024

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Association between infant breastfeeding practices and timing of peak height velocity: A nationwide longitudinal survey in Japan.
Yousuke Higuchi, Naomi Matsumoto, Shintaro Fujiwara, Yuki Ebuchi, Mahoko Furujo

Pediatr Res· November 2023

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A 4-month-old female infant with breast development and virilisation.
Shintaro Fujiwara, Yousuke Higuchi, Yuki Ebuchi, Yu Fukushima, Takahiro Ohkura, Mahoko Furujo

J Paediatr Child Health· March 2023

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Effect of growth hormone therapy on thyroid function in isolated growth hormone deficient and short small for gestational age children: a two-year study, including on assessment of the usefulness of the thyrotropin-releasing hormone (TRH) stimulation test.
Yuki Ebuchi, Toshihide Kubo, Mahoko Furujo, Yousuke Higuchi, Shoko Fujinaga

J Pediatr Endocrinol Metab· November 2020

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A 9-year-old girl with Kawasaki disease and pulmonary nodules.
Yousuke Higuchi, Motoharu Ochi, Junya Shimizu, Mahoko Furujo

Clin Rheumatol· October 2020

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Generation of a human induced pluripotent stem cell line, BRCi001-A, derived from a patient with mucopolysaccharidosis type I.
Mika Suga, Takayuki Kondo, Keiko Imamura, Ran Shibukawa, Yasue Okanishi, Mahoko Furujo

Stem Cell Res· April 2019

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Hypertensive Cerebral Hemorrhage in a Patient with Turner Syndrome Caused by Deletion in the Short Arm of the X Chromosome.
Yusuke S Hori, Takahiro Ohkura, Yuki Ebisudani, Michiari Umakoshi, Masato Ishi, Mahoko Furujo

Pediatr Neurosurg· September 2018

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Intrathecal Baclofen Pump Implantation for Type 2 Gaucher Disease.
Yusuke S Hori, Toru Fukuhara, Mizuho Aoi, Motoharu Ochi, Mahoko Furujo

Pediatr Neurosurg· June 2018

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Effects of Growth Hormone Treatment on Lipid Profiles.
Toshihide Kubo, Mahoko Furujo, Kyohei Takahashi, Yuki Hyodo, Hiroki Tsuchiya

Indian J Pediatr· April 2018

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Enzyme replacement therapy attenuates disease progression in two Japanese siblings with mucopolysaccharidosis type VI: 10-Year follow up.
Mahoko Furujo, Motomichi Kosuga, Torayuki Okuyama

Mol Genet Metab Rep· December 2017

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Parkinsonism in Association with Dihydropteridine Reductase Deficiency.
Yoshiaki Takahashi, Yasuhiro Manabe, Yumiko Nakano, Taijun Yunoki, Syoichiro Kono, Mahoko Furujo

Case Rep Neurol· February 2017

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Three cases of Japanese acromicric/geleophysic dysplasia with FBN1 mutations: a comparison of clinical and radiological features.
Kosei Hasegawa, Chikahiko Numakura, Hiroyuki Tanaka, Mahoko Furujo, Toshihide Kubo

J Pediatr Endocrinol Metab· January 2017

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Usefulness of non-fasting lipid parameters in children.
Toshihide Kubo, Kyohei Takahashi, Mahoko Furujo, Yuki Hyodo, Hiroki Tsuchiya

J Pediatr Endocrinol Metab· January 2017

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Genetic and pharmacological correction of aberrant dopamine synthesis using patient iPSCs with BH4 metabolism disorders.
Taizo Ishikawa, Keiko Imamura, Takayuki Kondo, Yasushi Koshiba, Satoshi Hara, Mahoko Furujo

Hum Mol Genet· December 2016

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Clinical characteristics of epileptic seizures in a case of dihydropteridine reductase deficiency.
Mahoko Furujo, Masako Kinoshita, Yozo Ichiba, Anne Romstad, Haruo Shintaku

Epilepsy Behav Case Rep· February 2015

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An infant case of hyperprolactinemia induced by a functional disorder of the hypothalamus.
Toshihide Kubo, Mahoko Furujo

Clin Pediatr Endocrinol· May 2014

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Spectrum of mutations associated with methionine adenosyltransferase I/III deficiency among individuals identified during newborn screening in Japan.
Masayoshi Nagao, Toju Tanaka, Mahoko Furujo

Mol Genet Metab· December 2013

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Enzyme replacement therapy in two Japanese siblings with Fabry disease, and its effectiveness on angiokeratoma and neuropathic pain.
Mahoko Furujo, Toshihide Kubo, Masahisa Kobayashi, Toya Ohashi

Mol Genet Metab· November 2013

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Methionine adenosyltransferase I/III deficiency: neurological manifestations and relevance of S-adenosylmethionine.
Mahoko Furujo, Masako Kinoshita, Masayoshi Nagao, Toshihide Kubo

Mol Genet Metab· November 2012

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S-adenosylmethionine treatment in methionine adenosyltransferase deficiency, a case report.
Mahoko Furujo, Masako Kinoshita, Masayoshi Nagao, Toshihide Kubo

Mol Genet Metab· March 2012

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Enzyme replacement therapy attenuates disease progression in two Japanese siblings with mucopolysaccharidosis type VI.
Mahoko Furujo, Toshihide Kubo, Motomichi Kosuga, Torayuki Okuyama

Mol Genet Metab· December 2011

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Evaluation of partial body composition using bioelectrical impedance in Japanese children.
Toshihide Kubo, Kaoru Suzuki, Yukari Mimura, Mahoko Furujo, Hiroshi Shiraga

Asia Pac J Clin Nutr· February 2011

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Predicting obesity in early adulthood in Japanese women.
Toshihide Kubo, Mahoko Furujo, Yuko Ueda, Ken Imai, Kohei Tsukahara

J Paediatr Child Health· January 2008

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An infant case of macroprolactinemia with transient idiopathic central precocious puberty.
Toshihide Kubo, Mahoko Furujo, Shigehiro Mori, Ken Imai, Yuko Ueda

Endocr J· December 2007

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An infant case of Graves' disease with ophthalmopathy.
Toshihide Kubo, Junya Shimizu, Mahoko Furujo, Akihito Takeuchi, Haruna Yoshioka-Iwaso

Endocr J· October 2005

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