Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

3,728 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Multiplex Real-Time PCR-Based Newborn Screening for Severe Primary Immunodeficiency and Spinal Muscular Atrophy in Osaka, Japan: Our Results after 3 Years.
Kimizu T, Nozaki M, Okada Y, Sawada A, Morisaki M, Fujita H, Irie A, Matsuda K, Hasegawa Y, Nishi E, Okamoto N, Kawai M, Imai K, Suzuki Y, Wada K, Mitsuda N, Ida S. Kimizu T, et al. Among authors: matsuda k. Genes (Basel). 2024 Feb 28;15(3):314. doi: 10.3390/genes15030314. Genes (Basel). 2024. PMID: 38540372 Free PMC article.
Newborn screening for spinal muscular atrophy in Osaka -challenges in a Japanese pilot study.
Kimizu T, Ida S, Oki K, Shima M, Nishimoto S, Nakajima K, Ikeda T, Mogami Y, Yanagihara K, Matsuda K, Nishi E, Hasegawa Y, Nozaki M, Fujita H, Irie A, Katayama T, Okamoto N, Imai K, Nishio H, Suzuki Y. Kimizu T, et al. Among authors: matsuda k. Brain Dev. 2023 Aug;45(7):363-371. doi: 10.1016/j.braindev.2023.03.004. Epub 2023 Mar 25. Brain Dev. 2023. PMID: 36973114
Co-occurrence of Prader-Willi and Sotos syndromes.
Okamoto N, Akimaru N, Matsuda K, Suzuki Y, Shimojima K, Yamamoto T. Okamoto N, et al. Among authors: matsuda k. Am J Med Genet A. 2010 Aug;152A(8):2103-9. doi: 10.1002/ajmg.a.33544. Am J Med Genet A. 2010. PMID: 20635407
Delineation of dermatan 4-O-sulfotransferase 1 deficient Ehlers-Danlos syndrome: observation of two additional patients and comprehensive review of 20 reported patients.
Shimizu K, Okamoto N, Miyake N, Taira K, Sato Y, Matsuda K, Akimaru N, Ohashi H, Wakui K, Fukushima Y, Matsumoto N, Kosho T. Shimizu K, et al. Among authors: matsuda k. Am J Med Genet A. 2011 Aug;155A(8):1949-58. doi: 10.1002/ajmg.a.34115. Epub 2011 Jul 8. Am J Med Genet A. 2011. PMID: 21744491 Review.
A case of pulmonary tuberculosis that developed during nivolumab and ipilimumab treatment for pulmonary adenocarcinoma that recurred two months after completion of anti-tuberculous treatment.
Hirano S, Takahashi H, Nakamura S, Matsuda K, Ishikawa R, Tamura K, Shikano K, Fujita T, Amano H, Nakamura M. Hirano S, et al. Among authors: matsuda k. Chin Clin Oncol. 2024 May 31:cco-23-153. doi: 10.21037/cco-23-153. Online ahead of print. Chin Clin Oncol. 2024. PMID: 38859608 Free article.
Clinical and molecular features of patients with IDH1 wild-type primary glioblastoma presenting unexpected short-term survival after gross total resection.
Toyoda M, Shibahara I, Shigeeda R, Fujitani K, Tanihata Y, Hyakutake Y, Handa H, Komai H, Sato S, Inukai M, Hide T, Shimoda Y, Kanamori M, Endo H, Saito R, Matsuda KI, Sonoda Y, Kumabe T. Toyoda M, et al. Among authors: matsuda ki. J Neurooncol. 2024 Jun 5. doi: 10.1007/s11060-024-04687-2. Online ahead of print. J Neurooncol. 2024. PMID: 38839702
3,728 results