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原著
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1. Tanaka T, Niimi H, Matsuo N, Fujieda K,
Tachibana K, Ohyama K, Satoh M, Kugu K: Results of long-term
follow-up after treatment of central precocious puberty with
leuprorelin acetate:Evaluation of effectiveness of treatmetn
and recovery of gonadal function. J Clin Endocrinol
Metab,90:1371-1376, 2005
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2. Hanew K, Tachibana K, Yokoya S, Fujieda
K, Tanaka T, Igarashi Y, Shimatsu A, Tanaka H, Tanizawa
T, Teramoto A, Nishi Y, Hasegawa Y, Hizuka N, Hirano T,
Fujita K:Studies of very severe short stature with s
evere GH deficiency:From the data registered with the
Foundation for Growth Science. Endocrine J 52:37-43, 2005
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Zimmermann MB, Ito Y, Hess SY,
Fujieda K, Molinari L: Oncreased thyroid volume
innchildren with high dietry iodine intake. Am J
Clin Nutr 81:840-844, 2005
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Tajima T, Satoh K,
Okuhara K, Tsubaki J, Fujieda K: Hypomagnesemia
in a patient with Barth syndrome.J Pediatr
Endocrinol Metab 18:523, 2005
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Tajima T, Tsubaki J,
Fujieda K:Two novel mutations in the
thyroid peroxidase gene with goitrous
hypothyroidis. Endocr J 52:643-645, 2005
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Tanaka T, Tachibana K,
Shimatsu A, Katsumata N, Tsushima T, Hizuka N,
Fujieda K, Yokoya S, Irie M: A nationeide attempt
to standardize growth hormone assays. Horm Res 64(Supple2):6-11, 2005
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Tsuchiya E, Oki J, Yahara N,
Fujieda K: Computerized version of the
Wisconsin Card Shorting Test in children with
high-functioning autistic disorder and
attention-deficit/hyperactivity Disorder.
Brain and Development, 27:233-236, 2005
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Zhao C, Shuke N, Yamamoto W, Okizaki
A, Sato J, Kajino H, Fujieda K, Aburano T: Impaired
cardiac sympathetic nerve function in patients with
Kawasaki disease: Comparison with myocardial
perfusion. Pediatr Res 57:744-748, 2005
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Matsuyama M, Mizusaki H, Shimono
A, Mukai T, Okumura K, Abe K, Shimada K, Morohashi
K:A novel isoform of Vinexin, Vinexin γ, regulates
Sox9 gene expression through activation of MAPK
cascade in mouse fetal gonad。 Genes to Cells 18:
421-434, 2005
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Franzese A, Brunetti-Pierri
N, Spadaro R, Mukai T, Valerio G: Inappropriate
tall stature and renal ectopy in a male patient
with X-linked congenital adrenal hypoplasia due
to a novel missense mutation in the DAX-1 gene。
Am J Med Genet。 135A: 72-74, 2005
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Wakida N, Do Gia Tuyen, Adachi
M, Miyoshi T, Nonoguchi H, Oka T, Ueda O, Tazawa M,
Kurihara S, Yoneta Y, Shimada H, Oda T。 Kikushi Y,
Matsuo H, Hosoyamada M, Endou H, Otagiri M, Tomita K,
Kitamura K: Mutations in human urate transporter
1 gene in presecretory reabsorption defect type of
familial renal hypouricemia, J Clin Endocrinol
Metab 90: 2169-2174, 2005
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Suzuki S, Mukai T, Uetake K,
Sageshima S, Matsuo K, Ueda O, Ito Y, Fujieda K:
Permanent Neonatal Diabetes Mellitus with Growth
Disturbance, Developmental Delay, Epilepsy and
Dysmorphic Features, Clin Pediatr Endocrinol
14(suppl 24): 81-84, 2005
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Takahashi S, Ohshima T,
Cho A, Sreenath T, Iadarola MJ, Pant HC, Kim
Y, Nairn AC, Brady RO, Greengard P, Kulkarni
AB: Increased activity of cyclin-dependent
kinase 5 leads to attenuation of
cocaine-mediated dopamine signaling,
Proc Natl Acad Sci USA 102: 1737-1742, 2005
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Kohyama J, Hasegawa T.
Ohinata JS, Furushima W, Miyata R, Sugawara
H, Araki S: Obstructive sleep apnea and
insulin resistance in Japanese children,
Sleep and Biological Rhythms 3: 106-113, 2005
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Zhao C, Shuke N,
Yamamoto W, Okizaki A, Sato J, Kajino
H, Fujieda K, Aburano T:Impaired cardiac
sympathetic nerve function in patients
with Kawasaki disease: comparison with
myocardial perfusion. Pediatr Res. 57(5):744-8, 2005
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Kurotaki N, Shen JJ, Touyama M,
Kondoh T, Visser R, Ozaki T, Nishimoto J, Shiihara
T, Uetake K, Makita Y, Harada N, Raskin S, Brown CW,
Hoglund P, Okamoto N, Lupski JR: Phenotypic consequences
of genetic variation at hemizygous alleles: Sotos syndrome
is a contiguous gene syndrome incorporating coagulation
factor twelve (FXII) deficiency, Genetics in Medicine
Genet Med 7:479-483, 2005
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Udaka T, Samejima H, Kosaki R,
Kurosawa K, Okamoto N, Mizuno S, Makita Y, Numabe
H, Toral JF, Takahashi T, Kosaki K: Comprehensive
screening of CREB-binding protein gene mutations
among patients with Rubinstein-Taybi syndrome
using denaturing high-performance liquid
chromatography, Congenit Anom (Kyoto) 45:125-31, 2005
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宮田理英、大日向純子、神山潤、
林雅晴:色素性乾皮症の神経症状,医学のあゆみ 214:201-204,2005
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中山憲司、斉藤明子、西村一彦、桂英二、
市原修、鈴木智宏、孝口祐一、加藤芳伸、澤田幸司、
田村正秀、本間寛、小林邦彦、有賀正、藤枝憲二、
青木継稔:3歳児健診を利用したウイルソン病
スクリーニング、日本マス・スクリーニング学会雑誌
15:41-46, 2005
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松尾公美浩、鈴木滋、上田修、
向井徳男、伊藤善也、藤枝憲二:北海道におけるビタミンD
欠乏性くる病の発症の現状、北海道小児保健研究会会誌平成17年度:
45-47, 2005
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田中肇:特集:
子どもの眠り;より効果的なケアを実践するために
ー障害児の睡眠障害,小児看護 24:1489-1493,
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梶野浩樹:先天性心疾患(心室中隔欠損)
成長曲線は語る 成長障害をきたす小児疾患-症例と解説
藤枝憲二編、p214-215、診断と治療社
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林時仲、岡本年男、中村英記、長屋建、
竹田津原野、藤枝憲二:ハイリスク児のRSウイルス下気道感染症
に対するパリビズマブの予防効果、日本小児科学会雑誌
109(3);359-362,2005
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長屋建、田中真也、北島博之、藤村正哲:
新生児慢性肺疾患に対する十二指腸チューブ栄養の効果、
大阪府立母子保健総合医療センター雑誌20(2);51-54,2005
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加藤直樹、長尾竜兵、河島尚志、
有瀧健太郎、中島みずほ、篠本雅人、星加明徳、沼部博直、
蒔田芳男、島 義雄:グリクラジドが著効した新生児一過
性糖尿病の一例、小児科 46:1211-1215, 2005
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