Ohashi H - Search Results

1

Hyperechoic renal medullary pyramids in a boy with Simpson-Golabi-Behmel syndrome.

Nakane T, Sawanobori E, Ohashi H, Sugita K. Nakane T, et al. Among authors: ohashi h. Clin Dysmorphol. 2018 Jan;27(1):25-26. doi: 10.1097/MCD.0000000000000195. Clin Dysmorphol. 2018. PMID: 28746062 No abstract available.

2

[Williams syndrome].

Ohashi H. Ohashi H. Nihon Rinsho. 2005 Jul;63(7):1185-9. Nihon Rinsho. 2005. PMID: 16001780 Japanese.

3

[Cockayne syndrome].

Ohashi H. Ohashi H. Nihon Rinsho. 2006 Sep 28;Suppl 3:413-5. Nihon Rinsho. 2006. PMID: 17022576 Review. Japanese. No abstract available.

4

[XXX syndrome].

Ohashi H. Ohashi H. Nihon Rinsho. 2006 Jun 28;Suppl 2:522-4. Nihon Rinsho. 2006. PMID: 16817456 Review. Japanese. No abstract available.

5

20p11.23-p11.21 deletion in a child with hyperinsulinemic hypoglycemia and GH deficiency: A case report.

Sugawara D, Matsuura M, Sato H, Ohashi H, Ichihashi K. Sugawara D, et al. Among authors: ohashi h. Clin Pediatr Endocrinol. 2021;30(3):133-137. doi: 10.1297/cpe.30.133. Epub 2021 Jul 10. Clin Pediatr Endocrinol. 2021. PMID: 34285455 Free PMC article.

6

Single-Exon Deletions of ZNRF3 Exon 2 Cause Congenital Adrenal Hypoplasia.

Amano N, Narumi S, Aizu K, Miyazawa M, Okamura K, Ohashi H, Katsumata N, Ishii T, Hasegawa T. Amano N, et al. Among authors: ohashi h. J Clin Endocrinol Metab. 2024 Feb 20;109(3):641-648. doi: 10.1210/clinem/dgad627. J Clin Endocrinol Metab. 2024. PMID: 37878959

7

Efficacy of Antiseizure Medications in Wolf-Hirschhorn Syndrome.

Horiguchi A, Koichihara R, Kikuchi K, Nonoyama H, Daida A, Oba D, Hirata Y, Matsuura R, Ohashi H, Hamano SI. Horiguchi A, et al. Among authors: ohashi h. Neuropediatrics. 2023 Oct;54(5):339-343. doi: 10.1055/a-2077-1988. Epub 2023 Apr 19. Neuropediatrics. 2023. PMID: 37075791

8

Hypoplasia of abdominal wall muscles following massive fetal persistent chylous ascites without anemia.

Yamaguchi T, Tamaru S, Takano N, Sato K, Sakurai H, Ohashi H, Kamei Y. Yamaguchi T, et al. Among authors: ohashi h. Oxf Med Case Reports. 2021 Jun 18;2021(6):omab039. doi: 10.1093/omcr/omab039. eCollection 2021 Jun. Oxf Med Case Reports. 2021. PMID: 34158955 Free PMC article.

9

Novel compound heterozygous mutations in UHRF1 are associated with atypical immunodeficiency, centromeric instability and facial anomalies syndrome with distinctive genome-wide DNA hypomethylation.

Unoki M, Velasco G, Kori S, Arita K, Daigaku Y, Yeung WKA, Fujimoto A, Ohashi H, Kubota T, Miyake K, Sasaki H. Unoki M, et al. Among authors: ohashi h. Hum Mol Genet. 2023 Apr 20;32(9):1439-1456. doi: 10.1093/hmg/ddac291. Hum Mol Genet. 2023. PMID: 36458887

10

A Small-for-Gestational-Age Infant with MIRAGE Syndrome Who Developed Heat Stroke and Rhabdomyolysis due to Severe Temperature Instability.

Saito K, Nakagawa R, Narumi S, Ohashi H, Ishiguro A, Kabe K. Saito K, et al. Among authors: ohashi h. Neonatology. 2023;120(3):390-394. doi: 10.1159/000529762. Epub 2023 Apr 12. Neonatology. 2023. PMID: 37044079

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