Ohyama Y - Search Results

1

Congenital goiter sustaining normal level of serum triiodothyronine.

Nagasaka A, Nighei N, Hirooka Y, Mitsuma T, Kataoka K, Nakagawa H, Ohyama Y, Nakai A, Aono T, Iwase K, et al. Nagasaka A, et al. Among authors: ohyama y. Horm Metab Res. 1986 Dec;18(12):862-6. doi: 10.1055/s-2007-1012457. Horm Metab Res. 1986. PMID: 3817751

2

Congenital euthyroid goitre with impaired thyroglobulin transport.

Ohyama Y, Hosoya T, Kameya T, Suzuki N, Nakamura S, Kazahari K, Shibayama K, Yokota Y, Matsuura N. Ohyama Y, et al. Clin Endocrinol (Oxf). 1994 Jul;41(1):129-35. doi: 10.1111/j.1365-2265.1994.tb03794.x. Clin Endocrinol (Oxf). 1994. PMID: 8050126

3

Two novel cysteine substitutions (C1263R and C1995S) of thyroglobulin cause a defect in intracellular transport of thyroglobulin in patients with congenital goiter and the variant type of adenomatous goiter.

Hishinuma A, Takamatsu J, Ohyama Y, Yokozawa T, Kanno Y, Kuma K, Yoshida S, Matsuura N, Ieiri T. Hishinuma A, et al. Among authors: ohyama y. J Clin Endocrinol Metab. 1999 Apr;84(4):1438-44. doi: 10.1210/jcem.84.4.5633. J Clin Endocrinol Metab. 1999. PMID: 10199792

4

Expression of mRNA coding for pituitary hormones and pituitary-specific transcription factor in the pituitary gland of the rdw rat with hereditary dwarfism.

Shibayama K, Ohyama Y, Ono M, Furudate S. Shibayama K, et al. Among authors: ohyama y. J Endocrinol. 1993 Aug;138(2):307-13. doi: 10.1677/joe.0.1380307. J Endocrinol. 1993. PMID: 8228739

5

Assays for thyroid-stimulating antibodies and thyrotropin-binding inhibitory immunoglobulins in children with Graves' disease.

Shibayama K, Ohyama Y, Yokota Y, Ohtsu S, Takubo N, Matsuura N. Shibayama K, et al. Among authors: ohyama y. Endocr J. 2005 Oct;52(5):505-10. doi: 10.1507/endocrj.52.505. Endocr J. 2005. PMID: 16284425 Free article.

6

Rescue from dwarfism by thyroid function compensation in rdw rats.

Furudate S, Ono M, Shibayama K, Ohyama Y, Kuwada M, Kimura T, Kameya T. Furudate S, et al. Among authors: ohyama y. Exp Anim. 2005 Oct;54(5):455-60. doi: 10.1538/expanim.54.455. Exp Anim. 2005. PMID: 16365524 Free article.

7

The mechanisms of transient hypothyroxinemia in infants born to mothers with Graves' disease.

Matsuura N, Harada S, Ohyama Y, Shibayama K, Fukushi M, Ishikawa N, Yuri K, Nakanishi M, Yokota Y, Kazahari K, Oguchi H. Matsuura N, et al. Among authors: ohyama y. Pediatr Res. 1997 Aug;42(2):214-8. doi: 10.1203/00006450-199708000-00014. Pediatr Res. 1997. PMID: 9262225

8

High prevalence of T354P sodium/iodide symporter gene mutation in Japanese patients with iodide transport defect who have heterogeneous clinical pictures.

Kosugi S, Sato Y, Matsuda A, Ohyama Y, Fujieda K, Inomata H, Kameya T, Isozaki O, Jhiang SM. Kosugi S, et al. Among authors: ohyama y. J Clin Endocrinol Metab. 1998 Nov;83(11):4123-9. doi: 10.1210/jcem.83.11.5229. J Clin Endocrinol Metab. 1998. PMID: 9814502

9

Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene.

Shibayama K, Ohyama Y, Hishinuma A, Yokota Y, Kazahari K, Kazahari M, Ieiri T, Matsuura N. Shibayama K, et al. Among authors: ohyama y. Pediatr Int. 2005 Feb;47(1):105-8. doi: 10.1111/j.1442-200x.2005.02020.x. Pediatr Int. 2005. PMID: 15693879 No abstract available.

10

Ontogenic expression of somatostatin-messenger RNA in the intestinal tract of neonatal rats.

Yin XY, Koshimizu T, Yokota Y, Shibayama K, Ohyama Y, Yashiro K. Yin XY, et al. Among authors: ohyama y. Acta Paediatr Jpn. 1992 Feb;34(1):6-11. doi: 10.1111/j.1442-200x.1992.tb00917.x. Acta Paediatr Jpn. 1992. PMID: 1349787

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