Ohashi H - Search Results

1

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

2

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

3

Adapted whole-body surveillance for von Hippel-Lindau-associated tumors in 3p deletion syndrome with VHL deletion: A case report.

Morisawa K, Sato T, Shimoyamada M, Mizuno R, Ohashi H, Watanabe-Hisazumi H, Takeshima K, Kojima A, Sato S, Hasegawa T, Takahashi T. Morisawa K, et al. Among authors: ohashi h. Pediatr Blood Cancer. 2022 Nov;69(11):e29732. doi: 10.1002/pbc.29732. Epub 2022 Apr 19. Pediatr Blood Cancer. 2022. PMID: 35441425 No abstract available.

4

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.

5

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.

6

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

7

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.

8

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

9

RASopathies and spinal deformities for screening of scoliosis.

Machida M, Rocos B, Ohashi H, Taira K, Nemoto N, Oikawa N, Kaguchi R, Nakanishi K. Machida M, et al. Among authors: ohashi h. Pediatr Int. 2023 Jan-Dec;65(1):e15589. doi: 10.1111/ped.15589. Pediatr Int. 2023. PMID: 37615376

10

[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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,431 results

Search Page