Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Keiko Aso"'
Autor:
Keiko Aso, Takehiko Soutome, Mari Satoh, Takako Aoki, Hiromi Ogura, Toshiyuki Yamamoto, Hitoshi Kanno, Hiroyuki Takahashi
Publikováno v:
Clinical Case Reports, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract We report the case of a Filipino girl with autosomal‐recessive‐type distal renal tubular acidosis and Glanzmann thrombasthenia caused by homozygous variants in the genes SLC4A1 and ITGA2B within the long homozygous DNA region on chromoso
Externí odkaz:
https://doaj.org/article/ec906ab853de4f5094fb7371735416ec
Autor:
Yukiko Ueta1, Keiko Aso1, Youichi Haga1, Hiroyuki Takahashi1, Mari Satoh1 satomari@med.toho-u.ac.jp
Publikováno v:
Clinical Pediatric Endocrinology. 2022, Vol. 31 Issue 3, p159-162. 4p.
Publikováno v:
Endocrine journal.
5α-reductase type 2 (5αRD2) deficiency is a 46,XY disorder of sex development caused by impaired conversion of testosterone (T) to dihydrotestosterone (DHT). Penile enlargement therapy is important for male patients with 46,XY 5αRD2 deficiency who
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20083c4c21e1ba7e34fbd9d6975318b9
https://pubmed.ncbi.nlm.nih.gov/36216557
https://pubmed.ncbi.nlm.nih.gov/36216557
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 34:1191-1195
Objectives 5α-reductase type 2 deficiency due to biallelic SRD5A2 variants is a common form of 46,XY disorders of sex development. Case presentation A Chinese neonate presented with ambiguous genitalia. He carried a homozygous likely_pathogenic SRD5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9636968cd1eb62305f538b1fadd72be
https://doi.org/10.1515/jpem-2020-0678
https://doi.org/10.1515/jpem-2020-0678
Autor:
Keiko Aso, Mari Satoh
Publikováno v:
Endocrine Journal. 68:683-689
ACTH-cortisol dissociation is recognized in patients with critical illnesses. Cytokines, including tumor necrosis factor-α and interleukin-6 induce hypercortisolemia by enhancing the ACTH-independent synthesis and secretion of cortisol and by reduci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a2002ce84f1e59cbad7cf3e23b354e2
https://doi.org/10.1507/endocrj.ej20-0533
https://doi.org/10.1507/endocrj.ej20-0533
Publikováno v:
Pediatrics International. 64
Background The remission rate in children with Graves' disease (GD) after 2-6 years of antithyroid drug (ATD) treatment is 40-50%. It has been reported that it is difficult to predict the GD prognosis based on the TSH receptor antibody (TRAb) level a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df7a2c1be7d7478dca59953a3af733f1
https://doi.org/10.1111/ped.14749
https://doi.org/10.1111/ped.14749
Publikováno v:
Endocrine Journal; 2023, Vol. 70 Issue 1, p59-67, 9p
Publikováno v:
Endocrine Journal. 64:1173-1180
Thyroid disease is known to be associated with pulmonary arterial hypertension (PAH). We investigated the prevalence of thyroid disease in patients with idiopathic PAH (IPAH) or heritable PAH (HPAH), and the factors affecting the pathogenesis of thyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::651fe3e081632f3d1c4566b1ae824b7d
https://doi.org/10.1507/endocrj.ej17-0155
https://doi.org/10.1507/endocrj.ej17-0155
Autor:
Kazuya Sugitatsu, Tomoki Ochiai, Yutaka Tanaka, Shigeru Saito, Koki Shishido, Daisuke Hachinohe, Keiko Aso, Futoshi Yamanaka
Publikováno v:
Journal of Cardiology Cases. 13(2):63-66
Percutaneous transcatheter aortic valve implantation (TAVI), first introduced in 2002, is a viable solution for previously inoperable or high-risk patients with aortic stenosis, providing the benefit of valve replacement without the associated risks
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fedf2c3bb1c00039ddbcf6191875de18
Publikováno v:
Pediatrics International. 61:1053-1054
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e826c08000ce75ad049b1d2818b5966d
https://doi.org/10.1111/ped.13973
https://doi.org/10.1111/ped.13973