Ichihashi Y - Search Results

1

Destructive thyroiditis without autoantibodies in an infant.

Ichikawa Y, Sato T, Ichihashi Y, Ishii T, Hasegawa T. Ichikawa Y, et al. Among authors: ichihashi y. Pediatr Int. 2022 Jan;64(1):e14709. doi: 10.1111/ped.14709. Epub 2021 Oct 3. Pediatr Int. 2022. PMID: 34605112 No abstract available.

2

Testosterone priming increased growth hormone peak levels in the stimulation test and suppressed gonadotropin secretion in three Japanese adolescent boys.

Sato T, Kusakawa M, Ichihashi Y, Ishii T, Hasegawa T. Sato T, et al. Among authors: ichihashi y. Clin Pediatr Endocrinol. 2020;29(3):119-121. doi: 10.1297/cpe.29.119. Epub 2020 Jul 11. Clin Pediatr Endocrinol. 2020. PMID: 32694889 Free PMC article. No abstract available.

3

Case Report: Prenatal Genetic Counseling to Parents of Fetuses Suspected of Having Ambiguous Genitalia.

Sato T, Ishii T, Yamaguchi Y, Ichihashi Y, Ochiai D, Asanuma H, Kuroda T, Hasegawa T. Sato T, et al. Among authors: ichihashi y. Front Pediatr. 2021 Jan 13;8:569548. doi: 10.3389/fped.2020.569548. eCollection 2020. Front Pediatr. 2021. PMID: 33520882 Free PMC article.

4

Ultrasound finding of vaginal bleeding in infants with 21-hydroxylase deficiency.

Sato T, Ishii T, Ichihashi Y, Asanuma H, Hasegawa T. Sato T, et al. Among authors: ichihashi y. Pediatr Int. 2022 Jan;64(1):e14966. doi: 10.1111/ped.14966. Pediatr Int. 2022. PMID: 35112426 No abstract available.

5

Two novel mutations of COMP in Japanese boys with pseudoachondroplasia.

Ichihashi Y, Takagi M, Ishii T, Watanabe K, Nishimura G, Hasegawa T. Ichihashi Y, et al. Hum Genome Var. 2018 Jun 8;5:12. doi: 10.1038/s41439-018-0012-z. eCollection 2018. Hum Genome Var. 2018. PMID: 29899997 Free PMC article.

6

Hereditary paraganglioma presenting with atypical symptoms: Case report.

Eguchi S, Ono R, Sato T, Yada K, Umehara N, Narumi S, Ichihashi Y, Nozaki T, Kanomata N, Hasegawa T, Ozawa M, Hasegawa D. Eguchi S, et al. Among authors: ichihashi y. Medicine (Baltimore). 2021 Nov 19;100(46):e27888. doi: 10.1097/MD.0000000000027888. Medicine (Baltimore). 2021. PMID: 34797335 Free PMC article.

7

Discordant fetal phenotype of hypophosphatasia in two siblings.

Ikenoue S, Miyakoshi K, Ishii T, Sato Y, Otani T, Akiba Y, Kasuga Y, Ochiai D, Matsumoto T, Ichihashi Y, Matsuzaki Y, Tachikawa K, Michigami T, Nishimura G, Ikeda K, Hasegawa T, Tanaka M. Ikenoue S, et al. Among authors: ichihashi y. Am J Med Genet A. 2018 Jan;176(1):171-174. doi: 10.1002/ajmg.a.38531. Epub 2017 Nov 21. Am J Med Genet A. 2018. PMID: 29160033

8

Cover Image, Volume 176A, Number 1, January 2018.

Ikenoue S, Miyakoshi K, Ishii T, Sato Y, Otani T, Akiba Y, Kasuga Y, Ochiai D, Matsumoto T, Ichihashi Y, Matsuzaki Y, Tachikawa K, Michigami T, Nishimura G, Ikeda K, Hasegawa T, Tanaka M. Ikenoue S, et al. Among authors: ichihashi y. Am J Med Genet A. 2018 Jan;176(1):i. doi: 10.1002/ajmg.a.38585. Am J Med Genet A. 2018. PMID: 29232060

9

Transient Fanconi syndrome in two preterm infants with hydronephrosis and urinary tract infection.

Tominaga T, Sato T, Ichihashi Y, Amano N, Kobayashi Y, Awazu M. Tominaga T, et al. Among authors: ichihashi y. CEN Case Rep. 2017 May;6(1):88-90. doi: 10.1007/s13730-017-0250-9. Epub 2017 Feb 16. CEN Case Rep. 2017. PMID: 28509132 Free PMC article.

10

Child Abuse Prevention Team Activities in a General Hospital in Tochigi, Japan.

Kobayashi Y, Tsukui M, Ichihashi Y. Kobayashi Y, et al. Among authors: ichihashi y. Glob Pediatr Health. 2017 Nov 30;4:2333794X17743914. doi: 10.1177/2333794X17743914. eCollection 2017. Glob Pediatr Health. 2017. PMID: 29226188 Free PMC article. No abstract available.

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