MATSUO, Nobutake: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

1

Psychosomatic disorders in children: An emerging challenge to health care in Japan

Takao Takahashi, Hisako Watanabe, Nobutake Matsuo

Journal:

Pediatrics International

Year:

2002

Language:

english

File:

PDF, 155 KB

english, 2002

2

Effects of a Low-Volume Aerobic-Type Interval Exercise on V˙O2max and Cardiac Mass

MATSUO, TOMOAKI, SAOTOME, KOUSAKU, SEINO, SATOSHI, SHIMOJO, NOBUTAKE, MATSUSHITA, AKIRA, IEMITSU, MOTOYUKI, OHSHIMA, HIROSHI, TANAKA, KIYOJI, MUKAI, CHIAKI

Journal:

Medicine & Science in Sports & Exercise

Year:

2014

Language:

english

File:

PDF, 1.17 MB

english, 2014

3

Human Chorionic Gonadotropin Stimulation Test in Prepubertal Children with Micropenis Can Accurately Predict Leydig Cell Function in Pubertal or Postpubertal Adolescents

Ishii, Tomohiro, Matsuo, Nobutake, Sato, Seiji, Ogata, Tsutomu, Tamai, Shinya, Anzo, Makoto, Kamimaki, Tsutomu, Sasaki, Goro, Inokuchi, Mikako, Hori, Naoaki, Amano, Naoko, Narumi, Satoshi, Shibata, Hi

Journal:

Hormone Research in Paediatrics

Year:

2015

Language:

english

File:

PDF, 129 KB

english, 2015

4

Testicular volume in Japanese boys up to the age of 15 years

Nobutake Matsuo, Makoto Anzo, Seiji Sato, Tsutomu Ogata, Tsutomu Kamimaki

Journal:

European Journal of Pediatrics

Year:

2000

Language:

english

File:

PDF, 104 KB

english, 2000

5

Clinical and molecular studies in 15 females with ring X

Mari Matsuo, Koji Muroya, Masanori Adachi, Katsuhiko Tachibana, Yumi Asakura, Yoshiko Nakagomi, Keiichi Hanaki, Susumu Yokoya, Atsuko Yoshizawa, Yutaka Igarashi, Kunihiko Hanew, Nobutake Matsuo, Tsuto

Journal:

Year:

2000

Language:

english

File:

PDF, 60 KB

english, 2000

6

Sex determining gene on the X chromosome short arm: Dosage sensitive sex reversal

TSUTOMU OGATA, NOBUTAKE MATSUO

Journal:

Pediatrics International

Year:

1996

Language:

english

File:

PDF, 870 KB

english, 1996

7

Micropenis and the 5α-Reductase-2 (SRD5A2) Gene: Mutation and V89L Polymorphism Analysis in 81 Japanese Patients

Sasaki, Goro, Ogata, Tsutomu, Ishii, Tomohiro, Kosaki, Kenjiro, Sato, Seiji, Homma, Keiko, Takahashi, Takao, Hasegawa, Tomonobu, Matsuo, Nobutake

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2003

Language:

english

File:

PDF, 143 KB

english, 2003

8

Skeletal Features and Growth Patterns in 14 Patients with Haploinsufficiency of SHOX: Implications for the Development of Turner Syndrome

Kosho, Tomoki, Muroya, Koji, Nagai, Toshiro, Fujimoto, Masatoshi, Yokoya, Susumu, Sakamoto, Hiromi, Hirano, Takeki, Terasaki, Hiroshi, Ohashi, Hirofumi, Nishimura, Gen, Sato, Seiji, Matsuo, Nobutake,

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

1999

Language:

english

File:

PDF, 2.54 MB

english, 1999

9

Reference standard of penile size and prevalence of buried penis in Japanese newborn male infants

Matsuo, Nobutake, Ishii, Tomohiro, Takayama, John I, Miwa, Masayuki, Hasegawa, Tomonobu

Journal:

Endocrine Journal

Year:

2014

Language:

english

File:

PDF, 881 KB

english, 2014

10

WHO 2006 Child Growth Standards overestimate short stature and underestimate overweight in Japanese children

Inokuchi, Mikako, Matsuo, Nobutake, Takayama, John I., Hasegawa, Tomonobu

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2018

Language:

english

File:

PDF, 112 KB

english, 2018

11

Systemic lupus erythematosus in a patient with Noonan syndrome-like disorder with loose anagen hair 1: More than a chance association

Uehara, Tomoko, Hosogaya, Naoki, Matsuo, Nobutake, Kosaki, Kenjiro

Journal:

American Journal of Medical Genetics Part A

Year:

2018

Language:

english

File:

PDF, 492 KB

english, 2018

12

National anthropometric reference values and growth curves for Japanese children: history and critical review

Inokuchi, Mikako, Matsuo, Nobutake, Takayama, John I, Hasegawa, Tomonobu

Journal:

Annals of Human Biology

Year:

2019

Language:

english

File:

PDF, 878 KB

english, 2019

13

Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: Implication for the MRX locus

Muroya, Koji, Ogata, Tsutomu, Matsuo, Nobutake, Nagai, Toshiro, Franco, Brunella, Ballabio, Andrea, Rappold, Gudrun, Sakura, Nobiro, Fukushima, Yoshimitsu

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 527 KB

english, 1996

14

Hepatic dysfunction in two sibs with Alström syndrome: Case report and review of the literature

Awazu, Midori, Tanaka, Tetsuya, Sato, Seiji, Anzo, Makoto, Higuchi, Masataka, Yamazaki, Kazuto, Matsuo, Nobutake

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 273 KB

english, 1997

15

Phenotypic discordance in monozygotic twins with 22q11.2 deletion

Yamagishi, Hiroyuki, Ishii, Chihiro, Maeda, Jun, Kojima, Yoshifumi, Matsuoka, Rumiko, Kimura, Misa, Takao, Atsuyoshi, Momma, Kazuo, Matsuo, Nobutake

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 59 KB

english, 1998

16

Digynic triploid infant surviving for 46 days

Hasegawa, Tomonobu, Harada, Naoki, Ikeda, Kazushige, Ishii, Tomohiro, Hokuto, Isamu, Kasai, Kenji, Tanaka, Mamoru, Fukuzawa, Ryuji, Niikawa, Norio, Matsuo, Nobutake

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 267 KB

english, 1999

17

X-linked lissencephaly with ambiguous genitalia: Delineation of further case

Tsutomu Ogata, Nobutake Matsuo, Nobuyoshi Hiraoka, Jun-Ichi Hata

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 186 KB

english, 2000

18

Standard growth curves for Japanese patients with Prader-Willi syndrome

Toshiro Nagai, Nobutake Matsuo, Yasushi Kayanuma, Hidefumi Tonoki, Yoshimitsu Fukushima, Hirofumi Ohashi, Takayasu Murai, Tomoko Hasegawa, Yoshikazu Kuroki, Norio Niikawa

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 391 KB

english, 2000

19

FISH analysis for apparently simple terminal deletions of the X chromosome: Identification of hidden structural abnormalities

Tsutomu Ogata, Nobutake Matsuo, Yoshimitsu Fukushima, Masakazu Saito, Osamu Nose, Norio Miharu, Shigeki Uehara, Bunpei Ishizuka

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 140 KB

english, 2001

20

Novel mutation of TBX3 in a Japanese family with Ulnar-Mammary syndrome: Implication for impaired sex development

Goro Sasaki, Tsutomu Ogata, Tomohiro Ishii, Tomonobu Hasegawa, Seiji Sato, Nobutake Matsuo

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 151 KB

english, 2002

21

Autopsy case of microcephalic osteodysplastic primordial “dwarfism” type II

Ryuji Fukuzawa, Seiji Sato, Michael J. Sullivan, Gen Nishimura, Tomonobu Hasegawa, Nobutake Matsuo

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 177 KB

english, 2002

22

A ring X chromosome, 46,Y,r(X)(p22.33q28), as a cause of extreme short stature in a male

Tsutomu Ogata, Nobutake Matsuo, Nobuyoshi Shimizu

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 444 KB

english, 1990

23

Oto-palato-digital syndrome, type II: Evidence for defective intramembranous ossification

Tsutomu Ogata, Nobutake Matsuo, Gen Nishimura, Hiroshi Hajikano

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 771 KB

english, 1990

24

Molecular study of the Prader-Willi syndrome: Deletion, RFLP, and phenotype analyses of 50 patients

Jun-Ichi Hamabe, Yoshimitsu Fukushima, Naoki Harada, Kyohko Abe, Nobutake Matsuo, Toshiro Nagai, Akira Yoshioka, Hidefumi Tonoki, Ryuichi Tsukino, Norio Niikawa

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 936 KB

english, 1991

25

Absent chondrodysplasia punctata in a male with an Xp terminal deletion involving the putative region for CDPX1 locus

Dr. Tsutomu Ogata, Peter Goodfellow, Christine Petit, Pierre Maroteaux, Nobutake Matsuo

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 862 KB

english, 1993

26

Broad proximal phalanx, facial anomalies, hallux valgus, and bronchomalacia: Additional case

Dr. Yoko Tanaka, Nobutake Matsuo, Gen Nishimura, Toshiro Nagai

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 168 KB

english, 1994

27

Novel mutations of the ACTH receptor gene in a female adult patient with adrenal unresponsiveness to ACTH

Tomohiro Ishii, Tsutomu Ogata, Goro Sasaki, Seiji Sato, Ei-ichi Kinoshita, Nobutake Matsuo

Journal:

Clinical Endocrinology

Year:

2000

Language:

english

File:

PDF, 108 KB

english, 2000

28

Genetic evidence for a novel gene(s) involved in urogenital development on 10q26

Ogata, Tsutomu, Muroya, Koji, Sasagawa, Isoji, Kosho, Tomoki, Wakui, Keiko, Sakazume, Satoru, Ito, Katsumi, Matsuo, Nobutake, Ohashi, Hirofumi, Nagai, Toshiro

Journal:

Kidney International

Year:

2000

Language:

english

File:

PDF, 343 KB

english, 2000

29

Complete mutation analysis panel of the 39 human HOX genes

Kenjiro Kosaki, Rika Kosaki, Taichi Suzuki, Hiroshi Yoshihashi, Takao Takahashi, Katsumi Sasaki, Masaru Tomita, William McGinnis, Nobutake Matsuo

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2002

Language:

english

File:

PDF, 432 KB

english, 2002

30

Characterization of the aryl hydrocarbon receptor repressor gene and association of its Pro185Ala polymorphism with micropenis

Hideki Fujita, Rika Kosaki, Hiroshi Yoshihashi, Tsutomu Ogata, Masaru Tomita, Tomonobu Hasegawa, Takao Takahashi, Nobutake Matsuo, Kenjiro Kosaki

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2002

Language:

english

File:

PDF, 600 KB

english, 2002

31

Sex chromosome aberrations and stature: deduction of the principal factors involved in the determination of adult height

Tsutomu Ogata, Nobutake Matsuo

Journal:

Year:

1993

Language:

english

File:

PDF, 1.25 MB

english, 1993

32

Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features

Tsutomu Ogata, Nobutake Matsuo

Journal:

Year:

1995

Language:

english

File:

PDF, 2.31 MB

english, 1995

33

Refinement of the locus for X-linked recessive chondrodysplasia punctata

Koji Muroya, Tsutomu Ogata, Gudrun Rappold, Albrecht Klink, Yutaka Nakahori, Yoshimitsu Fukushima, Katsuya Aizu, Nobutake Matsuo

Journal:

Year:

1995

Language:

english

File:

PDF, 317 KB

english, 1995

34

Similar proportion of sporadic cases in Cytochromeb558negative chronic granulomatous disease and Duchenne muscular dystrophy

Yoko Tanaka, Nobutake Matsuo, Tadatoshi Kuratsuji

Journal:

Journal of Human Genetics

Year:

1991

Language:

english

File:

PDF, 457 KB

english, 1991

35

Multiple polypoid masses in the gastrointestinal tract in patient with Menkes disease on copper-histidinate therapy

Goro Sasaki, Tomohiro Ishii, Seiji Sato, Ken Hoshino, Yasuhide Morikawa, Hiroko Kodama, Nobutake Matsuo, Takao Takahashi, Tomonobu Hasegawa

Journal:

European Journal of Pediatrics

Year:

2004

Language:

english

File:

PDF, 197 KB

english, 2004

36

Age-dependent percentile for waist circumference for Japanese children based on the 1992–1994 cross-sectional national survey data

Mikako Inokuchi, Nobutake Matsuo, Makoto Anzo, John Ichiro Takayama, Tomonobu Hasegawa

Journal:

European Journal of Pediatrics

Year:

2007

Language:

english

File:

PDF, 255 KB

english, 2007

37

Further clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner stigmata

T. Ogata, Tomonobu Hasegawa, Nobutake Matsuo

Journal:

Year:

1997

Language:

english

File:

PDF, 13 KB

english, 1997

38

Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinasePHKA2gene

Barbara Burwinkel, Lluis Amat, R. George F. Gray, Nobutake Matsuo, Koji Muroya, Kuniaki Narisawa, Ronald J. Sokol, M. A. Vilaseca, M. W. Kilimann

Journal:

Year:

1998

Language:

english

File:

PDF, 193 KB

english, 1998

39

Microphthalmia with linear skin defects syndrome in a mosaic female infant with monosomy for the Xp22 region: molecular analysis of the Xp22 breakpoint and the X-inactivation pattern

T. Ogata, Keiko Wakui, Koji Muroya, Hirofumi Ohashi, Nobutake Matsuo, Donna M. Brown, Takashi Ishii, Yoshimitsu Fukushima

Journal:

Year:

1998

Language:

english

File:

PDF, 90 KB

english, 1998

40

White coat hypertension in two adolescents

Yoshio Yamaguchi, M. Awazu, Seiji Matsuoka, Jun Maeda, Mitsuaki Tokumura, Yoshifumi Kojima, Nobutake Matsuo

Journal:

Pediatric Nephrology

Year:

1999

Language:

english

File:

PDF, 51 KB

english, 1999

41

Joint laxity, vitreoretinal degeneration, facial abnormalities, and generalized skeletal alterations: A new syndrome?

G. Nishimura, Tomonobu Hasegawa, Kyoko Sugii, Kaiichiro Tsuyama, Nobutake Matsuo

Journal:

Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 273 KB

english, 1998

42

Genetic analysis of hypophosphatasia

SEIJI SATO, NOBUTAKE MATSUO

Journal:

Pediatrics International

Year:

1997

Language:

english

File:

PDF, 639 KB

english, 1997

43

Early initiation of L-dopa therapy enables stable development of executive function in tetrahydrobiopterin (BH4) deficiency

Yoko Tanaka, Motoichiro Kato, Taro Muramatsu, Fumie Saito, Seiji Sato, Nobutake Matsuo, Haruo Shintaku, Yoshiyuki Okano, Hiroshi Kondo, Tatsushi Nukazawa

Journal:

Developmental Medicine & Child Neurology

Year:

2007

Language:

english

File:

PDF, 91 KB

english, 2007

44

Body mass index reference values (mean and SD) for Japanese children

Mikako Inokuchi, Nobutake Matsuo, Makoto Anzo, Tomonobu Hasegawa

Journal:

Acta Paediatrica

Year:

2007

Language:

english

File:

PDF, 289 KB

english, 2007

45

Fetal testis formation: A critical event for sex determination and differentiation

NOBUTAKE MATSUO

Journal:

Pediatrics International

Year:

1996

Language:

english

File:

PDF, 226 KB

english, 1996

46

Mutations in the PIT-1 gene in children with combined pituitary hormone deficiency

Kohji Ohta, Yoshitaka Nobukuni, Hiroshi Mitsubuchi, Shigehiro Fujimoto, Nobutake Matsuo, Hiroshi Inagaki, Fumio Endo, Ichiro Matsuda

Journal:

Biochemical and Biophysical Research Communications

Year:

1992

Language:

english

File:

PDF, 352 KB

english, 1992

47

Serum lipolytic activity in Reye's syndrome

Ellen S. Kang, Nobutake Matsuo, Toshiro Nagai, Jack Greenhaw, Pamela L. Williams

Journal:

Clinica Chimica Acta

Year:

1989

Language:

english

File:

PDF, 556 KB

english, 1989

48

Enzyme reactor for urinary acylcarnitines assay by reversed-phase high-performance liquid chromatography

Kojiro Matsumoto, Mamoru Takahashi, Nobuaki Takiyama, Hideo Misaki, Nobutake Matsuo, Sawao Murano, Hidetaka Yuki

Journal:

Clinica Chimica Acta

Year:

1993

Language:

english

File:

PDF, 646 KB

english, 1993

49

Absent circadian variation of blood pressure in patients with anorexia nervosa

Midori Awazu, Seiji Matsuoka, Tsutomu Kamimaki, Hisako Watanabe, Nobutake Matsuo

Journal:

The Journal of Pediatrics

Year:

2000

Language:

english

File:

PDF, 814 KB

english, 2000

50

Fluorescence-based DHPLC for allelic quantification by single-nucleotide primer extension

Kenjiro Kosaki, Hiroshi Yoshihashi, Yuko Ohashi, Rika Kosaki, Taichi Suzuki, Nobutake Matsuo

Journal:

Journal of Biochemical and Biophysical Methods

Year:

2001

Language:

english

File:

PDF, 182 KB

english, 2001