Chiho Sugisawa
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Explore the profile of Chiho Sugisawa including associated specialties, affiliations and a list of published articles.
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33
Citations
157
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Recent Articles
1.
Abe K, Koizumi M, Kogai T, Ida S, Sugisawa C, Kawai M, et al.
Thyroid
. 2025 Feb;
PMID: 39895319
encodes sodium-iodide symporter (NIS), which transports inorganic iodide into thyroid cells. Biallelic loss-of-function variants in cause thyroid dyshormonogenesis due to iodide transport defect (ITD). We report a Japanese sibling with...
2.
Narumi S, Nagasaki K, Kiriya M, Uehara E, Akiba K, Tanase-Nakao K, et al.
Nat Genet
. 2024 May;
56(5):869-876.
PMID: 38714868
Insufficient thyroid hormone production in newborns is referred to as congenital hypothyroidism. Multinodular goiter (MNG), characterized by an enlarged thyroid gland with multiple nodules, is usually seen in adults and...
3.
Tanase-Nakao K, Iwahashi-Odano M, Sugisawa C, Abe K, Muroya K, Yamamoto Y, et al.
J Clin Endocrinol Metab
. 2024 Feb;
109(9):2358-2365.
PMID: 38373250
Context: Thyroglobulin (Tg), encoded by TG, is essential for thyroid hormone synthesis. TG defects result in congenital hypothyroidism (CH). Most reported patients were born before the introduction of newborn screening...
4.
Murai N, Saito N, Oka R, Nii S, Nishikawa H, Suzuki A, et al.
Metab Syndr Relat Disord
. 2024 Jan;
22(2):151-159.
PMID: 38190317
The present study aimed to clarify the relationships between novel and traditional anthropometric indices and insulin sensitivity (SI) in young and middle-aged Japanese persons with normal glucose tolerance (NGT), and...
5.
Sugisawa C, Narumi S, Tanase-Nakao K, Hoshiyama A, Suzuki N, Ohye H, et al.
Thyroid
. 2023 Feb;
33(5):556-565.
PMID: 36792927
More than 40 years have passed since the introduction of newborn screening (NBS) for congenital hypothyroidism (CH), and many early diagnosed patients have reached adulthood. Their thyroid morphology and function...
6.
Iizaka T, Kodama E, Mikura K, Iida T, Imai H, Hashizume M, et al.
Endocr J
. 2022 Sep;
70(1):69-76.
PMID: 36171144
Familial partial lipodystrophy (FPLD) 3 is a rare genetic disorder caused by peroxisome proliferator-activated receptor γ gene (PPARG) mutations. Most cases have been reported in Western patients. Here, we describe...
7.
Murai N, Saito N, Nii S, Nishikawa Y, Suzuki A, Kodama E, et al.
Metabol Open
. 2022 Jun;
15:100196.
PMID: 35733612
Aims: The present study aimed to clarify the relationships between diabetic family history (FH), and dysglycemic response to the oral glucose tolerance test (OGTT), insulin secretion, and insulin sensitivity in...
8.
Kubo H, Tsurutani Y, Sugisawa C, Sunouchi T, Hirose R, Saito J
Tohoku J Exp Med
. 2022 Jun;
257(4):337-345.
PMID: 35732416
Carney complex is a rare, autosomal dominant disease accompanied by multiple endocrine neoplastic syndromes. Mutations in the PRKAR1A gene have recently been reported as a cause of Carney complex, but...
9.
Narumi S, Opitz R, Nagasaki K, Muroya K, Asakura Y, Adachi M, et al.
Hum Mol Genet
. 2022 May;
31(23):3967-3974.
PMID: 35535691
Congenital hypothyroidism due to thyroid dysgenesis (TD), presented as thyroid aplasia, hypoplasia or ectopia, is one of the most prevalent rare diseases with an isolated organ malformation. The pathogenesis of...
10.
Mikura K, Kodama E, Iida T, Imai H, Hashizume M, Kigawa Y, et al.
J Diabetes Investig
. 2022 Mar;
13(8):1357-1365.
PMID: 35271762
Aims/introduction: This study examined the association between the severity of diabetic polyneuropathy (DPN) based on the Baba classification, and sarcopenia and its related factors. Materials And Methods: The participants were...