Kondo D - Search Results

1

Familial episodic limb pain in kindreds with novel Nav1.9 mutations.

Kabata R, Okuda H, Noguchi A, Kondo D, Fujiwara M, Hata K, Kato Y, Ishikawa K, Tanaka M, Sekine Y, Hishikawa N, Mizukami T, Ito J, Akasaka M, Sakurai K, Yoshida T, Minoura H, Hayashi T, Inoshita K, Matsuyama M, Kinjo N, Cao Y, Inoue S, Kobayashi H, Harada KH, Youssefian S, Takahashi T, Koizumi A. Kabata R, et al. Among authors: kondo d. PLoS One. 2018 Dec 17;13(12):e0208516. doi: 10.1371/journal.pone.0208516. eCollection 2018. PLoS One. 2018. PMID: 30557356 Free PMC article.

2

Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families.

Okuda H, Noguchi A, Kobayashi H, Kondo D, Harada KH, Youssefian S, Shioi H, Kabata R, Domon Y, Kubota K, Kitano Y, Takayama Y, Hitomi T, Ohno K, Saito Y, Asano T, Tominaga M, Takahashi T, Koizumi A. Okuda H, et al. Among authors: kondo d. PLoS One. 2016 May 25;11(5):e0154827. doi: 10.1371/journal.pone.0154827. eCollection 2016. PLoS One. 2016. PMID: 27224030 Free PMC article. Clinical Trial.

3

A novel S269C mutation in fibroblast growth factor receptor 3 in a Japanese child with hypochondroplasia.

Takahashi I, Kondo D, Oyama C, Yano T, Tamura H, Noguchi A, Takahashi T. Takahashi I, et al. Among authors: kondo d. Hum Genome Var. 2018 Apr 12;5:1. doi: 10.1038/s41439-018-0001-2. eCollection 2018. Hum Genome Var. 2018. PMID: 29736252 Free PMC article.

4

Elevated Urinary Levels of 8-Hydroxy-2'-deoxyguanosine in a Japanese Child of Xeroderma Pigmentosum/Cockayne Syndrome Complex with Infantile Onset of Nephrotic Syndrome.

Kondo D, Noguchi A, Tamura H, Tsuchida S, Takahashi I, Kubota H, Yano T, Oyama C, Sawaishi Y, Moriwaki S, Takahashi T. Kondo D, et al. Tohoku J Exp Med. 2016 Jul;239(3):231-5. doi: 10.1620/tjem.239.231. Tohoku J Exp Med. 2016. PMID: 27396511 Free article.

5

A novel ZC4H2 gene mutation, K209N, in Japanese siblings with arthrogryposis multiplex congenita and intellectual disability: characterization of the K209N mutation and clinical findings.

Kondo D, Noguchi A, Takahashi I, Kubota H, Yano T, Sato Y, Toyono M, Sawaishi Y, Takahashi T. Kondo D, et al. Brain Dev. 2018 Oct;40(9):760-767. doi: 10.1016/j.braindev.2018.05.003. Epub 2018 May 24. Brain Dev. 2018. PMID: 29803542

6

An Early-Onset Neuronopathic Form of Acid Sphingomyelinase Deficiency: A SMPD1 p.C133Y Mutation in the Saposin Domain of Acid Sphingomyelinase.

Ota S, Noguchi A, Kondo D, Nakajima Y, Ito T, Arai H, Takahashi T. Ota S, et al. Among authors: kondo d. Tohoku J Exp Med. 2020 Jan;250(1):5-11. doi: 10.1620/tjem.250.5. Tohoku J Exp Med. 2020. PMID: 31941852 Free article.

7

[Round table conference. Digestive tract diseases].

Kondo D, Nakayama T, Ishikawa K, Tsuneoka K. Kondo D, et al. Naika. 1966 Jun;17(6):1116-35. Naika. 1966. PMID: 5964529 Japanese. No abstract available.

8

[Round table conference: progress in medical care of enteropathy].

Tsuneoka K, Kondo D, Nagao F, Niwa H, Ishikawa M. Tsuneoka K, et al. Among authors: kondo d. Naika. 1971 Dec;28(6):1078-95. Naika. 1971. PMID: 5146223 Japanese. No abstract available.

9

[EARLY DIAGNOSIS OF STOMACH CANCER BY ENDOSCOPY WITH SPECIAL REFERENCE TO FIBERGLASS GASTROSCOPY].

TSUNEOKA K, TAKEMOTO T, FUKUCHI S, MATSUMOTO M, HIRATSUKA H, UCHIDA T, NAKAJIMA Y, KONDO D. TSUNEOKA K, et al. Among authors: kondo d. Naika. 1964 Sep;14:237-46. Naika. 1964. PMID: 14205740 Japanese. No abstract available.

10

[Effects of alcoholic drinks on the human stomach. 1].

Tanaka M, Takemoto T, Ichioka S, Obata Y, Kondo D. Tanaka M, et al. Among authors: kondo d. Nihon Shokakibyo Gakkai Zasshi. 1972 Jan;69(1):36-45. Nihon Shokakibyo Gakkai Zasshi. 1972. PMID: 4676636 Japanese. No abstract available.

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