Výsledky vyhledávání - "Kazuo, Yamawaki"

Tolerability of partially and extensively hydrolysed milk formulas in children with cow's milk allergy

Autor: Chisato, Inuo, Kenichi, Tanaka, Yoichi, Nakajima, Kazuo, Yamawaki, Takeshi, Matsubara, Hiroshi, Iwamoto, Ikuya, Tsuge, Atsuo, Urisu, Yasuto, Kondo

Publikováno v: Asia Pacific journal of clinical nutrition. 28(1)

The safety and tolerability of hydrolysed cow's milk protein-based formulas, particularly partially hydrolysed formulas (pHFs), in children with cow's milk allergy (CMA) remain poorly understood. We evaluated the tolerability of hydrolysed cow's milk

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e2ecacead86b3187928a593d62f46f6d
https://pubmed.ncbi.nlm.nih.gov/30896414

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Oral Immunotherapy Using Partially Hydrolyzed Formula for Cow's Milk Protein Allergy: A Randomized, Controlled Trial

Autor: Chisato Inuo, Kenichi Tanaka, Atsuo Urisu, Yoichi Nakajima, Satoko Suzuki, Yasuto Kondo, Kazuo Yamawaki, Ikuya Tsuge

Background: Partially hydrolyzed cow’s milk protein-based formula (pHF) possesses low allergenicity. Here, we investigate the safety and efficacy of oral immunotherapy using pHF for children with cow’s milk protein allergy (CMPA). Objectives: A r

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3760cadfc36e937dc579bd87949e4b5e
https://europepmc.org/articles/PMC6262684/

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Multicolor flow-cytometric analysis of milk allergen-specific T-helper type 2 cells revealed coexpression of interleukin-4 with Foxp3

Autor: Kazuo Yamawaki, Ikuya Tsuge, Chisato Inuo, Yoichi Nakajima, Kenichi Tanaka, Takayasu Nomura, Atsuo Urisu, Yasuto Kondo, Tetsushi Yoshikawa

Publikováno v: Annals of allergy, asthmaimmunology : official publication of the American College of Allergy, Asthma,Immunology. 115(6)

Background Allergen-specific T-helper type 2 (T H 2) cells play an important role in the development of allergic inflammation; however, investigations of the properties of allergen-specific T cells have been challenging in humans. Despite clear evide

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52f4b2b9c5c4d4126a5f1041391fbadb
https://pubmed.ncbi.nlm.nih.gov/26507707

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Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndrome

Autor: Masashi Morishita, Tamae Ohye, Makiko Tsutsumi, Ikuya Tsuge, Hidehito Inagaki, Chisato Inuo, Kuniko Ieda, Takema Kato, Kazuo Yamawaki, Hiroki Kurahashi, Akinori Hayakawa, Yuji Mori

Publikováno v: Human Genome Variation

Ichthyosis prematurity syndrome (IPS) is a rare autosomal recessive disorder characterized by prematurity, a thick caseous scale at birth and lifelong atopic diathesis. Here, we describe the first Japanese case of IPS and report novel compound hetero

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76db9aa05a8fd58c3dc859e4ed75f1a1
https://pubmed.ncbi.nlm.nih.gov/27081519

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Comment

Autor: Kazuo, Yamawaki

Publikováno v: 国立民族学博物館調査報告 = Senri Ethnological Reports. 54:47-49

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=jairo_______::57ba17083aedc9f682cbf4f1c2af38ef
http://hdl.handle.net/10502/1803

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