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Results: 1-25 | 26-27
Results: 1-25/27
Mutation analysis of phenylketonuria in Yamagata prefecture, Japan
Authors: Kimura, T Ikeda, H Akaba, K Guldberg, P Guttler, F Maki, K Aikawa, S Hayasaka, K
Citation: T. Kimura et al., Mutation analysis of phenylketonuria in Yamagata prefecture, Japan, PEDIATR INT, 43(1), 2001, pp. 1-3
Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1
Authors: Miyoshi, O Yabe, R Wakui, K Fukushima, Y Koizumi, S Uchikawa, M Kajii, T Numakura, C Takahashi, S Hayasaka, K Niikawa, N
Citation: O. Miyoshi et al., Two cases of mosaic RhD blood-group phenotypes and paternal isodisomy for chromosome 1, AM J MED G, 104(3), 2001, pp. 250-256
Laser cooling of calcium ions by use of ultraviolet laser diodes: Significant induction of electron-shelving transitions
Authors: Toyoda, K Miura, A Urabe, S Hayasaka, K Watanabe, M
Citation: K. Toyoda et al., Laser cooling of calcium ions by use of ultraviolet laser diodes: Significant induction of electron-shelving transitions, OPTICS LETT, 26(23), 2001, pp. 1897-1899
A single ion as a nanoscopic probe of an optical field
Authors: Guthohrlein, GR Keller, M Hayasaka, K Lange, W Walther, H
Citation: Gr. Guthohrlein et al., A single ion as a nanoscopic probe of an optical field, NATURE, 414(6859), 2001, pp. 49-51
Laser cooling of Ca+ with an external-cavity ultraviolet diode laser
Authors: Hayasaka, K Urabe, S Watanabe, M
Citation: K. Hayasaka et al., Laser cooling of Ca+ with an external-cavity ultraviolet diode laser, JPN J A P 2, 39(7A), 2000, pp. L687-L689
A new form of total anomalous pulmonary venous connection with double drainage
Authors: Tanabe, S Nakasato, M Suzuki, H Ishikawa, A Fukasawa, M Hayasaka, K
Citation: S. Tanabe et al., A new form of total anomalous pulmonary venous connection with double drainage, PEDIATR INT, 42(4), 2000, pp. 369-371
Six-year disease-free survival of a patient with metastatic eyelid squamous cell carcinoma and colon adenocarcinoma after repeated postoperative adoptive immunotherapy
Authors: Kawamura, A Sekine, T Sekiguchi, M Yanoma, S Kaneko, A Haneda, T Moriya, Y Hayasaka, K Kakizoe, T
Citation: A. Kawamura et al., Six-year disease-free survival of a patient with metastatic eyelid squamous cell carcinoma and colon adenocarcinoma after repeated postoperative adoptive immunotherapy, JPN J CLIN, 30(6), 2000, pp. 267-271
Sonic hedgehog signal peptide mutation in a patient with holoprosencephaly
Authors: Kato, M Nanba, E Akaboshi, S Shiihara, T Ito, A Honma, T Tsuburaya, K Hayasaka, K
Citation: M. Kato et al., Sonic hedgehog signal peptide mutation in a patient with holoprosencephaly, ANN NEUROL, 47(4), 2000, pp. 514-516
Hemizygous mutation of the peripheral myelin protein 22 gene associated with Charcot-Marie-Tooth disease type 1
Authors: Numakura, C Lin, CQ Oka, N Akiguchi, I Hayasaka, K
Citation: C. Numakura et al., Hemizygous mutation of the peripheral myelin protein 22 gene associated with Charcot-Marie-Tooth disease type 1, ANN NEUROL, 47(1), 2000, pp. 101-103
Intravenous leiomyomatosis
Authors: Hayasaka, K Tanaka, Y Fujii, M Himi, K Negishi, N
Citation: K. Hayasaka et al., Intravenous leiomyomatosis, J COMPUT AS, 24(1), 2000, pp. 83-85
Heterogeneous mutations in the glycogen-debranching enzyme gene are responsible for glycogen storage disease type IIIa in Japan
Authors: Okubo, M Horinishi, A Takeuchi, M Suzuki, Y Sakura, N Hasegawa, Y Igarashi, T Goto, K Tahara, H Uchimoto, S Omichi, K Kanno, H Hayasaka, K Murase, T
Citation: M. Okubo et al., Heterogeneous mutations in the glycogen-debranching enzyme gene are responsible for glycogen storage disease type IIIa in Japan, HUM GENET, 106(1), 2000, pp. 108-115
Compound heterozygous patient with glycogen storage disease type III: Identification of two novel AGL mutations, a donor splice site mutation of Chinese origin and a 1-bp deletion of Japanese origin
Authors: Okubo, M Horinishi, A Suzuki, Y Murase, T Hayasaka, K
Citation: M. Okubo et al., Compound heterozygous patient with glycogen storage disease type III: Identification of two novel AGL mutations, a donor splice site mutation of Chinese origin and a 1-bp deletion of Japanese origin, AM J MED G, 93(3), 2000, pp. 211-214
Prader-Willi syndrome in a child with XYY
Authors: Honma, A Ishii, R Ito, A Kato, M Saitoh, S Hayasaka, K
Citation: A. Honma et al., Prader-Willi syndrome in a child with XYY, J HUM GENET, 44(6), 1999, pp. 412-413
Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridinediphosphate-glucuronosyltransferase gene in Japanese
Authors: Akaba, K Kimura, T Sasaki, A Tanabe, S Wakabayashi, T Hiroi, M Yasumura, S Maki, K Aikawa, S Hayasaka, K
Citation: K. Akaba et al., Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridinediphosphate-glucuronosyltransferase gene in Japanese, J HUM GENET, 44(1), 1999, pp. 22-25
Antibody mimicking an anti-E antibody that binds to patient's E negative red cells
Authors: Morio, A Kobayashi, D Hayasaka, K Saito, K Yamane, K Sasaki, M Yagihashi, A Watanabe, N
Citation: A. Morio et al., Antibody mimicking an anti-E antibody that binds to patient's E negative red cells, IMMUNOPH IM, 21(2), 1999, pp. 221-231
Conformal invariance of the D-particle effective action
Authors: Hayasaka, K Nakayama, R
Citation: K. Hayasaka et R. Nakayama, Conformal invariance of the D-particle effective action, PHYS LETT B, 463(2-4), 1999, pp. 181-187
Diffuse pachygyria with cerebellar hypoplasia: A milder form of microlissencephaly or a new genetic syndrome?
Authors: Kato, M Takizawa, N Yamada, S Ito, A Honma, T Hashimoto, M Saito, E Ohta, T Chikaoka, H Hayasaka, K
Citation: M. Kato et al., Diffuse pachygyria with cerebellar hypoplasia: A milder form of microlissencephaly or a new genetic syndrome?, ANN NEUROL, 46(4), 1999, pp. 660-663
Hepatic hemangioblastoma: An unusual presentation of von Hippel-Lindau disease
Authors: Hayasaka, K Tanaka, Y Satoh, T Mutoh, H
Citation: K. Hayasaka et al., Hepatic hemangioblastoma: An unusual presentation of von Hippel-Lindau disease, J COMPUT AS, 23(4), 1999, pp. 565-566
A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia
Authors: Kato, M Kimura, T Lin, CQ Ito, A Kodama, S Morikawa, T Soga, T Hayasaka, K
Citation: M. Kato et al., A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia, HUM GENET, 104(4), 1999, pp. 341-344
MR findings in primary retroperitoneal Schwannoma
Authors: Hayasaka, K Tanaka, Y Soeda, S Huppert, P Claussen, CD
Citation: K. Hayasaka et al., MR findings in primary retroperitoneal Schwannoma, ACT RADIOL, 40(1), 1999, pp. 78-82
Intermittent jaundice in patients with acute leukaemia: A common mutation of the bilirubin uridine-diphosphate glucuronosyltransferase gene among Asians
Authors: Kimura, T Akaba, K Ikegami, T Akiba, K Kanazawa, C Katsuura, M Shimizu, Y Imaizumi, M Lin, C Hayasaka, K
Citation: T. Kimura et al., Intermittent jaundice in patients with acute leukaemia: A common mutation of the bilirubin uridine-diphosphate glucuronosyltransferase gene among Asians, J INH MET D, 22(6), 1999, pp. 747-753
Deletion and nonsense mutations of the connexin 32 gene associated with Charcot-Marie-Tooth disease
Authors: Lin, CQ Numakura, C Ikegami, T Shizuka, M Shoji, M Nicholson, G Hayasaka, K
Citation: Cq. Lin et al., Deletion and nonsense mutations of the connexin 32 gene associated with Charcot-Marie-Tooth disease, TOH J EX ME, 188(3), 1999, pp. 239-244
A novel mutation of the myelin P-o gene segregating Charcot-Marie-Tooth disease type 1B manifesting as trigeminal nerve thickening
Authors: Shizuka, M Ikeda, Y Watanabe, M Okamoto, K Shoji, M Ikegami, T Hayasaka, K
Citation: M. Shizuka et al., A novel mutation of the myelin P-o gene segregating Charcot-Marie-Tooth disease type 1B manifesting as trigeminal nerve thickening, J NE NE PSY, 67(2), 1999, pp. 250-251
The effects of shading on translocation of C-13-photosynthates between lateral branches during the rapid growth period of cherry, pear, and Japanese persimmon fruit
Authors: Yamamoto, T Nobori, H Sasaki, H Hayasaka, K
Citation: T. Yamamoto et al., The effects of shading on translocation of C-13-photosynthates between lateral branches during the rapid growth period of cherry, pear, and Japanese persimmon fruit, J JPN S HOR, 68(2), 1999, pp. 302-311
CD48 expression on leukocytes in infectious diseases: Flow cytometric analysis of surface antigen
Authors: Katsuura, M Shimizu, Y Akiba, K Kanazawa, C Mitsui, T Sendo, D Kawakami, T Hayasaka, K Yokoyama, S
Citation: M. Katsuura et al., CD48 expression on leukocytes in infectious diseases: Flow cytometric analysis of surface antigen, ACT PAED J, 40(6), 1998, pp. 580-585
Risultati: 1-25 | 26-27