Komatsu H - Search Results

1

The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies.

Nozu K, Iijima K, Kanda K, Nakanishi K, Yoshikawa N, Satomura K, Kaito H, Hashimura Y, Ninchoji T, Komatsu H, Kamei K, Miyashita R, Kugo M, Ohashi H, Yamazaki H, Mabe H, Otsubo A, Igarashi T, Matsuo M. Nozu K, et al. Among authors: komatsu h. J Clin Endocrinol Metab. 2010 Dec;95(12):E511-8. doi: 10.1210/jc.2010-0392. Epub 2010 Sep 1. J Clin Endocrinol Metab. 2010. PMID: 20810575

2

De novo X-linked Alport syndrome in a 3-year-old girl.

Komatsu H, Goda T, Nozu K. Komatsu H, et al. BMJ Case Rep. 2019 Jul 15;12(7):e230183. doi: 10.1136/bcr-2019-230183. BMJ Case Rep. 2019. PMID: 31308192 Free PMC article.

3

An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2.

Goda T, Komatsu H, Nozu K, Nakajima H. Goda T, et al. Among authors: komatsu h. Clin Pediatr Endocrinol. 2020;29(3):127-130. doi: 10.1297/cpe.29.127. Epub 2020 Jul 11. Clin Pediatr Endocrinol. 2020. PMID: 32694891 Free PMC article. No abstract available.

4

A pediatric case of hypomagnesemia 1 (HOMG1) caused by novel compound heterozygous mutations in TRPM6.

Goda T, Komatsu H, Nozu K, Nakajima H. Goda T, et al. Among authors: komatsu h. Hum Genome Var. 2019 Mar 6;6:13. doi: 10.1038/s41439-019-0043-0. eCollection 2019. Hum Genome Var. 2019. PMID: 30911400 Free PMC article.

5

A prospective cohort study of ALI/ARDS in the Tohoku district of Japan (second report).

Endo S, Shibata S, Sato N, Hashiba E, Tajimi K, Saito K, Kawamae K, Nakane M, Murakawa M; Tohoku ALI Study Group. Endo S, et al. J Anesth. 2010 Jun;24(3):351-8. doi: 10.1007/s00540-010-0881-x. Epub 2010 Mar 27. J Anesth. 2010. PMID: 20349197

6

Clinical and genetic features of lysinuric protein intolerance in Japan.

Noguchi A, Nakamura K, Murayama K, Yamamoto S, Komatsu H, Kizu R, Takayanagi M, Okuyama T, Endo F, Takasago Y, Shoji Y, Takahashi T. Noguchi A, et al. Among authors: komatsu h. Pediatr Int. 2016 Oct;58(10):979-983. doi: 10.1111/ped.12946. Epub 2016 Jun 8. Pediatr Int. 2016. PMID: 26865117

7

Values for urinary beta 2-microglobulin and N-acetyl-beta-D-glucosaminidase in normal healthy infants.

Nishida M, Kawakatsu H, Komatsu H, Ishiwari K, Tamai M, Tsunamoto K, Kasubuchi Y, Sawada T. Nishida M, et al. Among authors: komatsu h. Acta Paediatr Jpn. 1998 Oct;40(5):424-6. doi: 10.1111/j.1442-200x.1998.tb01961.x. Acta Paediatr Jpn. 1998. PMID: 9821699

8

Efficacy of thyrotropin-releasing hormone in the treatment of spinal muscular atrophy.

Takeuchi Y, Miyanomae Y, Komatsu H, Oomizono Y, Nishimura A, Okano S, Nishiki T, Sawada T. Takeuchi Y, et al. Among authors: komatsu h. J Child Neurol. 1994 Jul;9(3):287-9. doi: 10.1177/088307389400900313. J Child Neurol. 1994. PMID: 7930408

9

Spinal muscular atrophy in trizygotic triplets.

Komatsu H, Takeuchi Y, Miyanomae Y, Yoshioka H, Daniels R, Davies KE, Sawada T. Komatsu H, et al. Acta Paediatr Jpn. 1994 Oct;36(5):522-6. doi: 10.1111/j.1442-200x.1994.tb03239.x. Acta Paediatr Jpn. 1994. PMID: 7825456

10

Monoamine metabolites in the cerebrospinal fluid in infantile spinal muscular atrophy.

Takeuchi Y, Komatsu H, Matsuo S, Hirai K, Kawase S, Nishimura A, Sawada T. Takeuchi Y, et al. Among authors: komatsu h. Neuroreport. 1994 Apr 14;5(8):898-900. doi: 10.1097/00001756-199404000-00011. Neuroreport. 1994. PMID: 8061291

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