Search Results - "Akihisa Nitta"

Perinatal and neonatal characteristics of Prader–Willi syndrome in Japan by Oto, Yuji, Murakami, Nobuyuki, Imatani, Kaishi, Inoue, Takeshi, Itabashi, Hisashi, Shiraishi, Masahisa, Nitta, Akihisa, Matsubara, Keiko, Kobayashi, Sayuki, Ihara, Hiroshi, Nagai, Toshiro, Matsubara, Tomoyo

“…Background Prader–Willi syndrome (PWS) is suspected at birth if extreme hypotonia, difficulty in feeding, hypogonadism, and failure to thrive are present…”
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Primary hyperparathyroidism in a child with abdominal pain and hematuria by Fukaya, Yuta, Oto, Yuji, Inoue, Takeshi, Itabashi, Hisashi, Shiraishi, Masahisa, Nitta, Akihisa, Murakami, Nobuyuki, Soh, Shigehiro, Ogawa, Toshihisa, Matsubara, Tomoyo

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Fetal Bone Formation Is Decreased from Middle Pregnancy to Birth by Nitta, Akihisa, Suzumura, Hiroshi, Arisaka, Osamu, Miura, Toshihide, Igarashi, Yoshihiko

“…Fetal bone development is a complex process that is regulated and maintained by minerals, hormones, and growth factors delivered from the mother via the…”
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Cardiopulmonary Arrest on Arrival in an Infant due to Ruptured Hepatoblastoma by Nitta, Akihisa, MD, Hisamatsu, Seito, MD, Fukuda, Hironobu, MD, PhD, Kurosawa, Hidemitsu, MD, PhD, Arisaka, Osamu, MD, PhD

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Thyroxine for transient hypothyroxinemia and cerebral palsy in extremely preterm infants by Suzumura, Hiroshi, Nitta, Akihisa, Tsuboi, Yayoi, Watabe, Yoshiyuki, Kuribayashi, Ryouta, Arisaka, Osamu

“…Background:  The relationship of thyroxine supplementation for transient hypothyroxinemia of prematurity to the incidence of cerebral palsy (CP) in infants <28…”
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Primary hyperparathyroidism in a child with abdominal pain and hematuria by Yuta Fukaya, Yuji Oto, Takeshi Inoue, Hisashi Itabashi, Masahisa Shiraishi, Akihisa Nitta, Nobuyuki Murakami, Shigehiro Soh, Toshihisa Ogawa, Tomoyo Matsubara

“…[Introduction] Primary hyperparathyroidism (PHPT) is an endocrine disease characterized by chronically elevated serum calcium and abnormally high PTH levels …”
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Fetal Hemophagocytic Lymphohistiocytosis in a Premature Infant by Nitta, Akihisa, MD, Suzumura, Hiroshi, MD, PhD, Watabe, Yoshiyuki, MD, PhD, Okuya, Mayuko, MD, PhD, Nakajima, Daisuke, MD, PhD, Kurosawa, Hidemitsu, MD, PhD, Sugita, Kenichi, MD, PhD, Arisaka, Osamu, MD, PhD

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Congenital cystic periventricular leukomalacia in a small‐for‐gestational age full‐term infant by Nitta, Akihisa, Suzumura, Hiroshi, Kano, Kenichi, Arisaka, Osamu

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An analysis of epilepsy with chromosomal abnormalities by Yamanouchi, Hideo, Imataka, George, Nakagawa, Eiji, Nitta, Akihisa, Suzuki, Naomitsu, Hirano, Jun-ichi, Suzumura, Hiroshi, Watanabe, Hiroshi, Arisaka, Osamu, Eguchi, Mitsuoki

“…We retrospectively reviewed the medical records of neonates with chromosomal abnormalities and epilepsy who had been admitted to the neonatal intensive care…”
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Diastolic flow velocity of the left pulmonary artery of patent ductus arteriosus in preterm infants by Suzumura, Hiroshi, Nitta, Akihisa, Tanaka, Goro, Arisaka, Osamu

“…Background : The usefulness of diastolic pulmonary flow velocity determined by echocardiography in the assessment of symptomatic patent ductus arteriosus…”
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Congenital left brachiocephalic vein and superior vena cava aneurysms in an infant: final update with autopsy findings by Nitta, Akihisa, MD, Nishikura, Kiyoshi, MD, Fukuda, Hironobu, MD, Yoshihara, Shigemi, MD, Hirao, Junichi, MD, Arisaka, Osamu, MD, Matsuda, Hadzki, MD

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A case report of odonto-hypophosphatasia with a novel variant in the ALPL gene by Oto, Yuji, Suzuki, Daiki, Morita, Tsubasa, Inoue, Takeshi, Nitta, Akihisa, Murakami, Nobuyuki, Abe, Yuuka, Hamada, Yoshinobu, Akiyama, Tomoyuki, Matsubara, Tomoyo

“…Hypophosphatasia (HPP) is a rare skeletal dysplasia caused by variants in the ( ) gene. More than 400 pathogenic variants of the gene have been registered in…”
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Systemic effects of transdermal testosterone for the treatment of microphallus in children by Arisaka, Osamu, Hoshi, Megumi, Kanazawa, Sanae, Nakajima, Daisuke, Numata, Michio, Nishikura, Kiyoshi, Oyama, Mariko, Nitta, Akihisa, Kuribayashi, Takeo, Kano, Kenichi, Nakayama, Yuko, Yamashiro, Yuichiro

“…Objectives : To elucidate the metabolic effects of topical testosterone for the treatment of microphallus in children. Methods : We administered 5%…”
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Discordant responses of bone formation and absorption markers in Japanese infants with vitamin D deficiency: a comprehensive matched case-control study by Takahashi, Keigo, Ikeda, Kazushige, Hara-Isono, Kaori, Nitta, Akihisa, Nagano, Nobuhiko, Arimitsu, Takeshi

“…Vitamin D deficiency during infancy has been associated with increased bone turnover rate and bone mineral loss. However, few studies have examined bone…”
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Role of infection in the development of acquired subglottic stenosis in neonates with prolonged intubation by Suzumura, Hiroshi, Nitta, Akihisa, Tanaka, Goro, Kuwashima, Shigeko

“…Objective: To examine whether clinically diagnosed infection correlates with subsequent development of subglottic stenosis in intubated neonates. Methods :…”
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Successful treatment of Gaucher disease type 1 by enzyme replacement therapy over a 10-year duration in a Japanese pediatric patient: A case report by Oto, Yuji, Inoue, Takeshi, Nagai, So, Tanaka, Shinichiro, Itabashi, Hisashi, Shiraisihi, Masahisa, Nitta, Akihisa, Murakami, Nobuyuki, Ida, Hiroyuki, Matsubara, Tomoyo

“…The prevalence of Gaucher disease (GD) in Japan is much lower than that in Western countries; therefore, data on Japanese pediatric patients with GD type 1 are…”
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Precocious Puberty Resulting from Congenital Hypothalamic Hamartoma: Persistent Darkened Areolae After Birth as the Hallmark of Estrogen Excess by Arisaka, Osamu, Negishi, Masao, Numata, Michio, Hoshi, Megumi, Kanazawa, Sanae, Oyama, Mariko, Nitta, Akihisa, Suzumuara, Hiroshi, Kuribayashi, Takeo, Nakayama, Yuko

“…Central precocious puberty due to congenital hypothalamic hamartoma may cause isosexual precocity from early infancy. To emphasize the importance of early…”
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Sequence Analysis of Thyroid Transcription Factor-2 (TTF-2) Gene in Ten Patients with Congenital Hypothyroidism due to Thyroid Dysgenesis by Kuribayashi, Takeo, Hishinuma, Akira, Kanazawa, Sanae, Nihei, Yuko, Hoshi, Megumi, Oyama, Mariko, Nitta, Akihisa, Ieiri, Tamio, Arisaka, Osamu

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Congenital toxoplasmosis complicated with central diabetes insipidus in the first week of life by Nitta, Akihisa, Suzumura, Hiroshi, Kano, Kenichi, Arisaka, Osamu

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Ngenital left brachiocephalic vein and superior vena cava aneurysms in an infant by NITTA, Akihisa, SUZUMURA, Hiroshi, KANO, Kenichi, ARISAKA, Osamu

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