Suzuki S - Search Results

1

Pediatric hypertrophic cardiomyopathy caused by a novel TNNI3 variant.

Inagaki N, Okano T, Kobayashi M, Fujii M, Yazaki Y, Takei Y, Kosuge H, Suzuki S, Hayashi T, Kuroda M, Satomi K. Inagaki N, et al. Among authors: suzuki s. Hum Genome Var. 2024 Mar 29;11(1):14. doi: 10.1038/s41439-024-00272-1. Hum Genome Var. 2024. PMID: 38548731 Free PMC article.

2

A family case of X-linked Alport syndrome patients with a novel variant in COL4A5.

Kashiwagi Y, Suzuki S, Agata K, Morishima Y, Inagaki N, Numabe H, Kawashima H. Kashiwagi Y, et al. Among authors: suzuki s. CEN Case Rep. 2019 May;8(2):75-78. doi: 10.1007/s13730-018-0368-4. Epub 2018 Oct 6. CEN Case Rep. 2019. PMID: 30293132 Free PMC article.

3

A Case of Primary Ciliary Dyskinesia Caused by a Mutation in OFD1, Which Was Diagnosed Owing to Clostridium difficile Infection.

Hasegawa R, Suzuki S, Nishimata S, Kashiwagi Y, Inagaki N, Kawashima H. Hasegawa R, et al. Among authors: suzuki s. Pediatr Rep. 2021 May 10;13(2):241-244. doi: 10.3390/pediatric13020033. Pediatr Rep. 2021. PMID: 34068458 Free PMC article.

4

Pathogenic variant of RBM20 in a multiplex family with hypertrophic cardiomyopathy.

Inagaki N, Hayashi T, Takei Y, Kosuge H, Suzuki S, Tanimoto K, Chikamori T, Kimura A. Inagaki N, et al. Among authors: suzuki s. Hum Genome Var. 2022 Feb 18;9(1):6. doi: 10.1038/s41439-022-00183-z. Hum Genome Var. 2022. PMID: 35181673 Free PMC article.

5

Case report: Rare heterozygous variant in the NR5A1 gene causing 46,XY complete gonadal dysgenesis with a non-communicating rudimentary uterus.

Sasaki T, Suzuki S, Ono M, Yamamoto A, Bingo M, Yamanaka G, Kuroda M, Inagaki N, Nishi H. Sasaki T, et al. Among authors: suzuki s. Front Med (Lausanne). 2024 Aug 1;11:1441990. doi: 10.3389/fmed.2024.1441990. eCollection 2024. Front Med (Lausanne). 2024. PMID: 39149602 Free PMC article.

6

Ferroportin Disease Caused by a Heterozygous Variant p.Cys326Phe in the SLC40A1 Gene and the Efficacy of Therapeutic Phlebotomy in Children.

Shimura M, Nishimata S, Saito N, Tsutsumi N, Suzuki S, Morishima Y, Kashiwagi Y, Numabe H, Kawashima H. Shimura M, et al. Among authors: suzuki s. J Pediatr Hematol Oncol. 2019 Jul;41(5):e325-e328. doi: 10.1097/MPH.0000000000001301. J Pediatr Hematol Oncol. 2019. PMID: 30130274

7

A Review on the Triggers of Pediatric Migraine with the Aim of Improving Headache Education.

Yamanaka G, Morichi S, Suzuki S, Go S, Takeshita M, Kanou K, Ishida Y, Oana S, Kawashima H. Yamanaka G, et al. Among authors: suzuki s. J Clin Med. 2020 Nov 19;9(11):3717. doi: 10.3390/jcm9113717. J Clin Med. 2020. PMID: 33228144 Free PMC article. Review.

8

Complementary and Integrative Medicines as Prophylactic Agents for Pediatric Migraine: A Narrative Literature Review.

Yamanaka G, Kanou K, Takamatsu T, Takeshita M, Morichi S, Suzuki S, Ishida Y, Watanabe Y, Go S, Oana S, Kawashima H. Yamanaka G, et al. Among authors: suzuki s. J Clin Med. 2021 Jan 3;10(1):138. doi: 10.3390/jcm10010138. J Clin Med. 2021. PMID: 33401551 Free PMC article. Review.

9

Clinical Features and Burden Scores in Japanese Pediatric Migraines With Brainstem Aura, Hemiplegic Migraine, and Retinal Migraine.

Yamanaka G, Go S, Morichi S, Takeshita M, Morishita N, Suzuki S, Tomoko T, Kasuga A, Daida A, Ishida Y, Oana S, Suganami Y, Nagao R, Kashiwagi Y, Kawashima H. Yamanaka G, et al. Among authors: suzuki s. J Child Neurol. 2020 Sep;35(10):667-673. doi: 10.1177/0883073820927840. Epub 2020 Jun 1. J Child Neurol. 2020. PMID: 32476572

10

A New Pathogenic Variant of CAKUTHED Diagnosed Based on Intellectual Disability.

Morichi S, Suzuki S, Kasuga A, Ishida Y, Yamanaka G, Kashiwagi Y, Kawashima H. Morichi S, et al. Among authors: suzuki s. Indian J Pediatr. 2020 Jun;87(6):480-481. doi: 10.1007/s12098-019-03091-3. Epub 2019 Nov 12. Indian J Pediatr. 2020. PMID: 31713835 No abstract available.

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