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Authors: NISHIMURA G HASEGAWA T SUGII K TSUYAMA K MATSUO N
Citation: G. Nishimura et al., JOINT LAXITY, VITREORETINAL DEGENERATION, FACIAL ABNORMALITIES, AND GENERALIZED SKELETAL ALTERATIONS - A NEW SYNDROME, JOURNAL OF HUMAN GENETICS, 43(3), 1998, pp. 191-194

Authors: NISHIMURA G NAGAI T
Citation: G. Nishimura et T. Nagai, A CASE OF CRANIOFACIAL DYSMORPHISM, CONGENITAL HEART-DEFECTS, COCCYGEAL SKIN FOLDS, GENERALIZED SKELETAL ALTERATIONS, AND HEMIHYPERTROPHY WITH LINEAR SKIN HYPOPIGMENTATION - A NEW SYNDROME, JOURNAL OF HUMAN GENETICS, 43(1), 1998, pp. 65-68

Authors: SATO T NISHIMURA G FUSHIDA S FUJIMURA T YONEMURA Y NONOMURA A MIWA K MIYAZAKI I
Citation: T. Sato et al., EVALUATION OF P53, KI-67 AND DNA-PLOIDY IN BOTH PRIMARY RECTAL CARCINOMAS AND LOCALLY RECURRENT TUMORS, Oncology Reports, 5(5), 1998, pp. 1225-1229

Authors: NISHIMURA G IWASAWA T FUKUZAWA R HIRABAYASHI Y ITO T
Citation: G. Nishimura et al., VARIABILITY OF PLATYSPONDYLIC LETHAL CHONDRODYSPLASIA - ANOTHER CASE-REPORT, Clinical dysmorphology, 7(3), 1998, pp. 195-200

Authors: NISHIMURA G SAITOH Y OKUZUMI S IMAIZUMI K HAYASAKA K HASHIMOTO M
Citation: G. Nishimura et al., SPONDYLOEPIPHYSEAL DYSPLASIA WITH ACCUMULATION OF GLYCOPROTEIN IN THECHONDROCYTES - SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE, Skeletal radiology, 27(4), 1998, pp. 188-194

Authors: NISHIMURA G SATOH M AIHARA T AIDA N YAMAMOTO T OZONO K
Citation: G. Nishimura et al., A DISTINCT SUBTYPE OF METATROPIC DYSPLASIA VARIANT CHARACTERIZED BY ADVANCED CARPAL SKELETAL AGE AND SUBLUXATION OF THE RADIAL HEADS, Pediatric radiology, 28(2), 1998, pp. 120-125

Authors: NISHIMURA G KUROSAWA K KOBAYASHI H KAWAME H
Citation: G. Nishimura et al., OSTEOGENESIS IMPERFECTA-LIKE SYNDROME WITH SEVERE MENTAL-RETARDATION AND EXTRAPYRAMIDAL TRACT SIGNS, Pediatric radiology, 28(11), 1998, pp. 856-858

Authors: NISHIMURA G NAKAYAMA M FUKE Y SUEHARA N
Citation: G. Nishimura et al., A LETHAL OSTEOCHONDRODYSPLASIA WITH MESOMELIC BRACHYMELIA, ROUND PELVIS, AND CONGENITAL HEPATIC-FIBROSIS - 2 SIBLINGS BORN TO CONSANGUINEOUS PARENTS, Pediatric radiology, 28(1), 1998, pp. 43-47

Authors: NISHIMURA G MIKAWA M FUKUSHIMA Y
Citation: G. Nishimura et al., ANOTHER OBSERVATION OF LANGER-TYPE SPONASTRIME DYSPLASIA VARIANT, American journal of medical genetics, 80(3), 1998, pp. 288-290

Authors: SUZUMURA H KANO K NISHIMURA G
Citation: H. Suzumura et al., HYPOPLASIA OF THE TRANSVERSE SINUS IN OTOPALATODIGITAL SYNDROME TYPE-I, American journal of medical genetics, 79(5), 1998, pp. 401-402

Authors: NISHIMURA G FUKUSHIMA Y AIHARA T OHASHI H NISHIMOTO H NISHIMURA J
Citation: G. Nishimura et al., PREVIOUSLY UNDESCRIBED SPONDYLOEPIPHYSEAL-DYSPLASIA ASSOCIATED WITH CRANIOSYNOSTOSIS, CATARACTS, CLEFT-PALATE, AND MENTAL-RETARDATION - REPORT OF 4 SIBS, American journal of medical genetics, 77(1), 1998, pp. 1-7

Authors: INOMATA N HOSHINO R NISHIMURA G
Citation: N. Inomata et al., INTRACTABLE APNEIC SPELLS DUE TO HYPOPLASIA OF THE ATLAS IN A PATIENTWITH UNCLASSIFIABLE SHORT-RIB DYSPLASIA, American journal of medical genetics, 76(3), 1998, pp. 276-278

Authors: KUWASHIMA S NISHIMURA G KONO T YAMATO M FUMITOSHI I FUJIOKA M
Citation: S. Kuwashima et al., MR ASSESSMENT FOR THE FETAL LUNG - DOES THE ABSENCE OF PULMONARY FETAL FLUID ON MR WARRANT A DIAGNOSIS OF PULMONARY HYPOPLASIA, Radiology, 209P, 1998, pp. 295-295

Authors: NISHIMURA G TSUKUDA M ZHOU LX FURUKAWA S BABA Y
Citation: G. Nishimura et al., CYCLIN D1 EXPRESSION AS A PROGNOSTIC FACTOR IN ADVANCED HYPOPHARYNGEAL CARCINOMA, Journal of Laryngology and Otology, 112(6), 1998, pp. 552-555

Authors: KINJO M NISHIMURA G KOYAMA T METS U RIGLER R
Citation: M. Kinjo et al., SINGLE-MOLECULE ANALYSIS OF RESTRICTION DNA FRAGMENTS USING FLUORESCENCE CORRELATION SPECTROSCOPY, Analytical biochemistry (Print), 260(2), 1998, pp. 166-172

Authors: NISHIMURA G YAMATO M TAMAI K TAKAHASHI J UETANI M
Citation: G. Nishimura et al., MR FINDINGS IN ILIOTIBIAL BAND SYNDROME, Skeletal radiology, 26(9), 1997, pp. 533-537

Authors: IWASAWA T TANAKA Y AIDA N OKUZUMI S NISHIHIRA H NISHIMURA G
Citation: T. Iwasawa et al., MICROSCOPIC INTRAOSSEOUS EXTENSION OF OSTEOSARCOMA - ASSESSMENT ON DYNAMIC CONTRAST-ENHANCED MRI, Skeletal radiology, 26(4), 1997, pp. 214-221

Authors: YAMATO M NISHIMURA G YAMAGUCHI T TAMAI K SAOTOME K
Citation: M. Yamato et al., EPITHELIOID SARCOMA WITH UNUSUAL RADIOLOGICAL FINDINGS, Skeletal radiology, 26(10), 1997, pp. 606-610

Authors: EHARA S KIM OH MAISAWA S TAKASAGO Y NISHIMURA G
Citation: S. Ehara et al., AXIAL SPONDYLOMETAPHYSEAL DYSPLASIA, European journal of pediatrics, 156(8), 1997, pp. 627-630

Authors: NISHIMURA G OKADA T TACHIBANA K ADACHI M MASUNO M IMAIZUMI K AIDA N
Citation: G. Nishimura et al., OSTEOPATHIA STRIATA, SHORT STATURE, AND CHARACTERISTIC FACIES - A PREVIOUSLY UNKNOWN SKELETAL DYSPLASIA, European journal of pediatrics, 156(8), 1997, pp. 631-635

Authors: NISHIMURA G MUGISHIMA H HIRAO J YAMATO M
Citation: G. Nishimura et al., GENERALIZED METAPHYSEAL MODIFICATION WITH CONE-SHAPED EPIPHYSES FOLLOWING LONG-TERM ADMINISTRATION OF 13-CIS-RETINOIC ACID, European journal of pediatrics, 156(6), 1997, pp. 432-435

Authors: KOBAYASHI N AIDA N NISHIMURA G KASHIMURA T OHTA M KAWATAKI M
Citation: N. Kobayashi et al., ACUTE GASTRIC OUTLET OBSTRUCTION FOLLOWING THE ADMINISTRATION OF PROSTAGLANDIN - AN ADDITIONAL CASE, Pediatric radiology, 27(1), 1997, pp. 57-59

Authors: AIDA N NISHIMURA G YAGISHITA A TAMAGAWA K
Citation: N. Aida et al., CEREBELLAR POLYMICROGYRIA - REPLY, American journal of neuroradiology, 18(2), 1997, pp. 394-395

Authors: NISHIMURA G HORIUCHI T KIM OH SASAMOTO Y
Citation: G. Nishimura et al., ATYPICAL SKELETAL CHANGES IN OTOPALATODIGITAL SYNDROME TYPE-II - PHENOTYPIC OVERLAP AMONG OTOPALATODIGITAL SYNDROME TYPE-II, BOOMERANG DYSPLASIA, ATELOSTEOGENESIS TYPE-I AND TYPE-III, AND LETHAL MALE PHENOTYPEOF MELNICK-NEEDLES-SYNDROME, American journal of medical genetics, 73(2), 1997, pp. 132-138

Authors: NISHIMURA G NISHIMURA J
Citation: G. Nishimura et J. Nishimura, MULTIPLE, JUXTASUTURAL, CRANIAL HYPEROSTOSES AND CARDIAC TUMOR - A NEW HAMARTOMATOUS SYNDROME, American journal of medical genetics, 71(2), 1997, pp. 167-171
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