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Items: 1 to 50 of 1262

1.

A case of a "pseudo jump-up phenomenon" caused by retrograde ventricular-His prolongation.

Ukita K, Egami Y, Matsunaga-Lee Y, Yanagawa K, Nakamura H, Matsuhiro Y, Yasumoto K, Tsuda M, Okamoto N, Tanaka A, Yano M, Yamato M, Shutta R, Nishino M, Tanouchi J.

J Electrocardiol. 2019 Nov 5;58:43-45. doi: 10.1016/j.jelectrocard.2019.11.003. [Epub ahead of print]

PMID:
31710874
2.

The Levels of Interferon-gamma Release as a Biomarker for Non-small-cell Lung Cancer Patients Receiving Immune Checkpoint Inhibitors.

Hirashima T, Kanai T, Suzuki H, Yoshida H, Matsushita A, Kawasumi H, Samejima Y, Noda Y, Nasu S, Tanaka A, Morishita N, Hashimoto S, Kawahara K, Tamura Y, Okamoto N, Tanaka T.

Anticancer Res. 2019 Nov;39(11):6231-6240. doi: 10.21873/anticanres.13832.

PMID:
31704852
3.

Electrochemical phase transformation accompanied with Mg extraction and insertion in a spinel MgMn2O4 cathode material.

Hatakeyama T, Okamoto NL, Shimokawa K, Li H, Nakao A, Uchimoto Y, Tanimura H, Kawaguchi T, Ichitsubo T.

Phys Chem Chem Phys. 2019 Nov 14;21(42):23749-23757. doi: 10.1039/c9cp04461b. Epub 2019 Oct 22.

PMID:
31637389
4.

Inter- and Intramolecular Alkyne-Carbonyl Metathesis/1,6-Addition/Oxidative Aromatization Tandem Reactions between 1,6-Diynes and Aldehydes.

Okamoto N, Sueda T, Minami H, Yanada R.

Org Lett. 2019 Nov 1;21(21):8847-8851. doi: 10.1021/acs.orglett.9b03494. Epub 2019 Oct 21.

PMID:
31633934
5.

Associated factors with delayed ambulation after abdominal surgery.

Asada J, Ida M, Sato M, Okamoto N, Kawaguchi M.

J Anesth. 2019 Oct 16. doi: 10.1007/s00540-019-02696-4. [Epub ahead of print]

PMID:
31620877
6.

Beneficial Effect of Pimobendan for Severe Heart Failure Due to Transthyretin Cardiac Amyloidosis.

Okamoto N, Kubo T, Nakashima Y, Ochi Y, Takahashi A, Baba Y, Hirota T, Yamasaki N, Kitaoka H.

Intern Med. 2019 Oct 7. doi: 10.2169/internalmedicine.3675-19. [Epub ahead of print]

7.

Missense Mutations in NKAP Cause a Disorder of Transcriptional Regulation Characterized by Marfanoid Habitus and Cognitive Impairment.

Fiordaliso SK, Iwata-Otsubo A, Ritter AL, Quesnel-Vallières M, Fujiki K, Nishi E, Hancarova M, Miyake N, Morton JEV, Lee S, Hackmann K, Bando M, Masuda K, Nakato R, Arakawa M, Bhoj E, Li D, Hakonarson H, Takeda R, Harr M, Keena B, Zackai EH, Okamoto N, Mizuno S, Ko JM, Valachova A, Prchalova D, Vlckova M, Pippucci T, Seiler C, Choi M, Matsumoto N, Di Donato N, Barash Y, Sedlacek Z, Shirahige K, Izumi K.

Am J Hum Genet. 2019 Nov 7;105(5):987-995. doi: 10.1016/j.ajhg.2019.09.009. Epub 2019 Oct 3.

PMID:
31587868
8.

Comparison of the Utilities of Cryobiopsy and Forceps Biopsy for Peripheral Lung Cancer.

Nasu S, Okamoto N, Suzuki H, Shiroyama T, Tanaka A, Samejima Y, Kanai T, Noda Y, Morita S, Morishita N, Ueda K, Kawahara K, Hirashima T.

Anticancer Res. 2019 Oct;39(10):5683-5688. doi: 10.21873/anticanres.13766.

PMID:
31570467
9.

Barrett's adenocarcinoma with esophageal varices successfully treated by endoscopic submucosal dissection with direct varices coagulation.

Ueda C, Yosizaki T, Katayama N, Okamoto N, Hashimura H, Matsumoto M, Takagi M, Ikeoka S, Momose K, Eguchi T, Yamashita H, Okada A.

Clin J Gastroenterol. 2019 Sep 26. doi: 10.1007/s12328-019-01048-9. [Epub ahead of print]

PMID:
31559540
10.

Involvement of Spermidine in the Reduced Lifespan of Caenorhabditis elegans During Vitamin B12 Deficiency.

Bito T, Okamoto N, Otsuka K, Yabuta Y, Arima J, Kawano T, Watanabe F.

Metabolites. 2019 Sep 19;9(9). pii: E192. doi: 10.3390/metabo9090192.

11.

Genetic abnormalities in a large cohort of Coffin-Siris syndrome patients.

Sekiguchi F, Tsurusaki Y, Okamoto N, Teik KW, Mizuno S, Suzumura H, Isidor B, Ong WP, Haniffa M, White SM, Matsuo M, Saito K, Phadke S, Kosho T, Yap P, Goyal M, Clarke LA, Sachdev R, McGillivray G, Leventer RJ, Patel C, Yamagata T, Osaka H, Hisaeda Y, Ohashi H, Shimizu K, Nagasaki K, Hamada J, Dateki S, Sato T, Chinen Y, Awaya T, Kato T, Iwanaga K, Kawai M, Matsuoka T, Shimoji Y, Tan TY, Kapoor S, Gregersen N, Rossi M, Marie-Laure M, McGregor L, Oishi K, Mehta L, Gillies G, Lockhart PJ, Pope K, Shukla A, Girisha KM, Abdel-Salam GMH, Mowat D, Coman D, Kim OH, Cordier MP, Gibson K, Milunsky J, Liebelt J, Cox H, El Chehadeh S, Toutain A, Saida K, Aoi H, Minase G, Tsuchida N, Iwama K, Uchiyama Y, Suzuki T, Hamanaka K, Azuma Y, Fujita A, Imagawa E, Koshimizu E, Takata A, Mitsuhashi S, Miyatake S, Mizuguchi T, Miyake N, Matsumoto N.

J Hum Genet. 2019 Dec;64(12):1173-1186. doi: 10.1038/s10038-019-0667-4. Epub 2019 Sep 17.

PMID:
31530938
12.

Bidirectional crosstalk between neutrophils and adipocytes promotes adipose tissue inflammation.

Watanabe Y, Nagai Y, Honda H, Okamoto N, Yanagibashi T, Ogasawara M, Yamamoto S, Imamura R, Takasaki I, Hara H, Sasahara M, Arita M, Hida S, Taniguchi S, Suda T, Takatsu K.

FASEB J. 2019 Nov;33(11):11821-11835. doi: 10.1096/fj.201900477RR. Epub 2019 Jul 29.

PMID:
31355683
13.

Comprehensive clinical and molecular studies in split-hand/foot malformation: identification of two plausible candidate genes (LRP6 and UBA2).

Yamoto K, Saitsu H, Nishimura G, Kosaki R, Takayama S, Haga N, Tonoki H, Okumura A, Horii E, Okamoto N, Suzumura H, Ikegawa S, Kato F, Fujisawa Y, Nagata E, Takada S, Fukami M, Ogata T.

Eur J Hum Genet. 2019 Dec;27(12):1845-1857. doi: 10.1038/s41431-019-0473-7. Epub 2019 Jul 22.

PMID:
31332306
14.

De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder.

Snijders Blok L, Kleefstra T, Venselaar H, Maas S, Kroes HY, Lachmeijer AMA, van Gassen KLI, Firth HV, Tomkins S, Bodek S; DDD Study, Õunap K, Wojcik MH, Cunniff C, Bergstrom K, Powis Z, Tang S, Shinde DN, Au C, Iglesias AD, Izumi K, Leonard J, Abou Tayoun A, Baker SW, Tartaglia M, Niceta M, Dentici ML, Okamoto N, Miyake N, Matsumoto N, Vitobello A, Faivre L, Philippe C, Gilissen C, Wiel L, Pfundt R, Deriziotis P, Brunner HG, Fisher SE.

Am J Hum Genet. 2019 Aug 1;105(2):403-412. doi: 10.1016/j.ajhg.2019.06.007. Epub 2019 Jul 11.

PMID:
31303265
15.

Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome.

Shoji Y, Ida S, Niihori T, Aoki Y, Okamoto N, Etani Y, Kawai M.

Endocr J. 2019 Jul 10. doi: 10.1507/endocrj.EJ18-0564. [Epub ahead of print]

16.

Increased risk of osteoporotic fracture in community-dwelling elderly men 20 or more years after gastrectomy: The Fujiwara-kyo Osteoporosis Risk in Men (FORMEN) Cohort Study.

Iki M, Fujita Y, Kouda K, Yura A, Tachiki T, Tamaki J, Sato Y, Moon JS, Hamada M, Kajita E, Okamoto N, Kurumatani N.

Bone. 2019 Oct;127:250-259. doi: 10.1016/j.bone.2019.06.014. Epub 2019 Jun 26.

PMID:
31254731
17.

A case of de novo splice site variant in SLC35A2 showing developmental delays, spastic paraplegia, and delayed myelination.

Miyamoto S, Nakashima M, Ohashi T, Hiraide T, Kurosawa K, Yamamoto T, Takanashi J, Osaka H, Inoue K, Miyazaki T, Wada Y, Okamoto N, Saitsu H.

Mol Genet Genomic Med. 2019 Aug;7(8):e814. doi: 10.1002/mgg3.814. Epub 2019 Jun 23.

18.

Crystal structure of η″-Fe3Al7+x determined by single-crystal synchrotron X-ray diffraction combined with scanning transmission electron microscopy.

Okamoto NL, Higashi M, Inui H.

Sci Technol Adv Mater. 2019 Jun 6;20(1):543-556. doi: 10.1080/14686996.2019.1613174. eCollection 2019.

19.

Relationship between tooth loss, low masticatory ability, and nutritional indices in the elderly: a cross-sectional study.

Okamoto N, Amano N, Nakamura T, Yanagi M.

BMC Oral Health. 2019 Jun 13;19(1):110. doi: 10.1186/s12903-019-0778-5.

20.

Stent Expansion and Endothelial Shear Stress in Bifurcation Lesions.

Okamoto N, Vengrenyuk Y, Bhatheja S, Chamaria S, Khan A, Gupta E, Kapur V, Barman N, Hasan C, Sweeny J, Baber U, Mehran R, Narula J, Sharma SK, Kini AS.

Circ Cardiovasc Interv. 2019 Jun;12(6):e007911. doi: 10.1161/CIRCINTERVENTIONS.119.007911. Epub 2019 Jun 14. No abstract available.

PMID:
31195824
21.

A case of successful concurrent anti-cancer treatment in a patient who developed follicular lymphoma during treatment with afatinib for advanced lung adenocarcinoma.

Masuhiro K, Koh G, Takata S, Nasu S, Takada H, Morita S, Tanaka A, Shiroyama T, Morishita N, Suzuki H, Okamoto N, Kawasumi H, Konishi C, Hirashima T.

Respir Med Case Rep. 2019 May 26;28:100862. doi: 10.1016/j.rmcr.2019.100862. eCollection 2019.

22.

Comprehensive analysis of coding variants highlights genetic complexity in developmental and epileptic encephalopathy.

Takata A, Nakashima M, Saitsu H, Mizuguchi T, Mitsuhashi S, Takahashi Y, Okamoto N, Osaka H, Nakamura K, Tohyama J, Haginoya K, Takeshita S, Kuki I, Okanishi T, Goto T, Sasaki M, Sakai Y, Miyake N, Miyatake S, Tsuchida N, Iwama K, Minase G, Sekiguchi F, Fujita A, Imagawa E, Koshimizu E, Uchiyama Y, Hamanaka K, Ohba C, Itai T, Aoi H, Saida K, Sakaguchi T, Den K, Takahashi R, Ikeda H, Yamaguchi T, Tsukamoto K, Yoshitomi S, Oboshi T, Imai K, Kimizu T, Kobayashi Y, Kubota M, Kashii H, Baba S, Iai M, Kira R, Hara M, Ohta M, Miyata Y, Miyata R, Takanashi JI, Matsui J, Yokochi K, Shimono M, Amamoto M, Takayama R, Hirabayashi S, Aiba K, Matsumoto H, Nabatame S, Shiihara T, Kato M, Matsumoto N.

Nat Commun. 2019 Jun 7;10(1):2506. doi: 10.1038/s41467-019-10482-9.

23.

Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders.

Yamamoto T, Imaizumi T, Yamamoto-Shimojima K, Lu Y, Yanagishita T, Shimada S, Chong PF, Kira R, Ueda R, Ishiyama A, Takeshita E, Momosaki K, Ozasa S, Akiyama T, Kobayashi K, Oomatsu H, Kitahara H, Yamaguchi T, Imai K, Kurahashi H, Okumura A, Oguni H, Seto T, Okamoto N.

Brain Dev. 2019 Oct;41(9):776-782. doi: 10.1016/j.braindev.2019.05.007. Epub 2019 Jun 4.

PMID:
31171384
24.

Germline-Activating RRAS2 Mutations Cause Noonan Syndrome.

Niihori T, Nagai K, Fujita A, Ohashi H, Okamoto N, Okada S, Harada A, Kihara H, Arbogast T, Funayama R, Shirota M, Nakayama K, Abe T, Inoue SI, Tsai IC, Matsumoto N, Davis EE, Katsanis N, Aoki Y.

Am J Hum Genet. 2019 Jun 6;104(6):1233-1240. doi: 10.1016/j.ajhg.2019.04.014. Epub 2019 May 23.

PMID:
31130285
25.

Skill-up study of systemic endoscopic examination technique using narrow band imaging of the head and neck region of patients with esophageal squamous cell carcinoma: Prospective multicenter study.

Okamoto N, Morimoto H, Yamamoto Y, Kanda K, Nankinzan R, Kasamatsu S, Yoshimura S, Kan M, Nakano A, Hosaka S, Watanabe Y, Arahata K, Toyama Y, Okamura A, Yamaguchi T, Yano T.

Dig Endosc. 2019 Nov;31(6):653-661. doi: 10.1111/den.13445. Epub 2019 Jun 20.

PMID:
31120161
26.

Therapeutic Potential of a Combination of Magnesium Hydroxide Nanoparticles and Sericin for Epithelial Corneal Wound Healing.

Nagai N, Iwai Y, Deguchi S, Otake H, Kanai K, Okamoto N, Shimomura Y.

Nanomaterials (Basel). 2019 May 19;9(5). pii: E768. doi: 10.3390/nano9050768.

27.

A single male auditory response test to quantify auditory behavioral responses in Drosophila melanogaster.

Ishikawa Y, Okamoto N, Yoneyama Y, Maeda N, Kamikouchi A.

J Neurogenet. 2019 Mar - Jun;33(2):64-74. doi: 10.1080/01677063.2019.1611805. Epub 2019 May 20.

PMID:
31106644
28.

Clinical and molecular spectrum of CHOPS syndrome.

Raible SE, Mehta D, Bettale C, Fiordaliso S, Kaur M, Medne L, Rio M, Haan E, White SM, Cusmano-Ozog K, Nishi E, Guo Y, Wu H, Shi X, Zhao Q, Zhang X, Lei Q, Lu A, He X, Okamoto N, Miyake N, Piccione J, Allen J, Matsumoto N, Pipan M, Krantz ID, Izumi K.

Am J Med Genet A. 2019 Jul;179(7):1126-1138. doi: 10.1002/ajmg.a.61174. Epub 2019 May 6.

PMID:
31058441
29.

Intravenous abatacept in Japanese patients with polyarticular-course juvenile idiopathic arthritis: results from a phase III open-label study.

Hara R, Umebayashi H, Takei S, Okamoto N, Iwata N, Yamasaki Y, Nakagishi Y, Kizawa T, Kobayashi I, Imagawa T, Kinjo N, Amano N, Takahashi Y, Mori M, Itoh Y, Yokota S.

Pediatr Rheumatol Online J. 2019 Apr 30;17(1):17. doi: 10.1186/s12969-019-0319-4.

30.

The frequency of cooking dinner at home and its association with nutrient intake adequacy among married young-to-middle-aged Japanese women: the POTATO Study.

Saito A, Matsumoto M, Hyakutake A, Saito M, Okamoto N, Tsuji M.

J Nutr Sci. 2019 Apr 22;8:e14. doi: 10.1017/jns.2019.9. eCollection 2019.

31.

Male CDPX2 patient with EBP mosaicism and asymmetrically lateralized skin lesions with strict midline demarcation.

Horinouchi T, Morisada N, Uemura H, Kobayashi D, Nozu K, Okamoto N, Iijima K.

Am J Med Genet A. 2019 Jul;179(7):1315-1318. doi: 10.1002/ajmg.a.61159. Epub 2019 Apr 29.

PMID:
31034146
32.

Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate.

Kato K, Miya F, Hori I, Ieda D, Ohashi K, Negishi Y, Hattori A, Okamoto N, Kato M, Tsunoda T, Yamasaki M, Kanemura Y, Kosaki K, Saitoh S.

J Hum Genet. 2019 Jul;64(7):701-702. doi: 10.1038/s10038-019-0610-8.

PMID:
31028281
33.

Clinical features and characteristics of uveitis associated with juvenile idiopathic arthritis in Japan: first report of the pediatric rheumatology association of Japan (PRAJ).

Yasumura J, Yashiro M, Okamoto N, Shabana K, Umebayashi H, Iwata N, Okura Y, Kubota T, Shimizu M, Tomiita M, Nakagishi Y, Nishimura K, Hara R, Mizuta M, Yasumi T, Yamaide F, Wakiguchi H, Kobayashi M, Mori M.

Pediatr Rheumatol Online J. 2019 Apr 11;17(1):15. doi: 10.1186/s12969-019-0318-5.

34.

Re-challenge chemotherapy in patients with sensitive relapse small-cell lung cancer and interstitial lung disease.

Nasu S, Suzuki H, Moriizumi K, Hara Y, Tanaka S, Takada H, Morita S, Tanaka A, Shiroyama T, Morishita N, Okamoto N, Hirashima T.

J Thorac Dis. 2019 Feb;11(2):514-520. doi: 10.21037/jtd.2019.01.26.

35.

Pathogenetic basis of Takenouchi-Kosaki syndrome: Electron microscopy study using platelets in patients and functional studies in a Caenorhabditis elegans model.

Uehara T, Suzuki H, Okamoto N, Kondoh T, Ahmad A, O'Connor BC, Yoshina S, Mitani S, Kosaki K, Takenouchi T.

Sci Rep. 2019 Mar 14;9(1):4418. doi: 10.1038/s41598-019-40988-7.

36.

Objective evaluation of the visibility of colorectal lesions using eye tracking.

Kumahara K, Ikematsu H, Shinmura K, Murano T, Inaba A, Okumura K, Nishihara K, Sunakawa H, Furue Y, Ito R, Sato D, Minamide T, Okamoto N, Yamamoto Y, Suyama M, Takashima K, Nakajo K, Yoda Y, Hori K, Oono Y, Yano T.

Dig Endosc. 2019 Sep;31(5):552-557. doi: 10.1111/den.13397. Epub 2019 Apr 8.

PMID:
30869814
37.

Genetic landscape of Rett syndrome-like phenotypes revealed by whole exome sequencing.

Iwama K, Mizuguchi T, Takeshita E, Nakagawa E, Okazaki T, Nomura Y, Iijima Y, Kajiura I, Sugai K, Saito T, Sasaki M, Yuge K, Saikusa T, Okamoto N, Takahashi S, Amamoto M, Tomita I, Kumada S, Anzai Y, Hoshino K, Fattal-Valevski A, Shiroma N, Ohfu M, Moroto M, Tanda K, Nakagawa T, Sakakibara T, Nabatame S, Matsuo M, Yamamoto A, Yukishita S, Inoue K, Waga C, Nakamura Y, Watanabe S, Ohba C, Sengoku T, Fujita A, Mitsuhashi S, Miyatake S, Takata A, Miyake N, Ogata K, Ito S, Saitsu H, Matsuishi T, Goto YI, Matsumoto N.

J Med Genet. 2019 Jun;56(6):396-407. doi: 10.1136/jmedgenet-2018-105775. Epub 2019 Mar 6.

PMID:
30842224
38.

Intellectual disability and dysmorphic features in male siblings arising from a novel TAF1 mutation.

Okamoto N, Arai H, Onishi T, Mizuguchi T, Matsumoto N.

Congenit Anom (Kyoto). 2019 Feb 25. doi: 10.1111/cga.12330. [Epub ahead of print] No abstract available.

PMID:
30805980
39.

Handling missing data in an FFQ: multiple imputation and nutrient intake estimates.

Ichikawa M, Hosono A, Tamai Y, Watanabe M, Shibata K, Tsujimura S, Oka K, Fujita H, Okamoto N, Kamiya M, Kondo F, Wakabayashi R, Noguchi T, Isomura T, Imaeda N, Goto C, Yamada T, Suzuki S.

Public Health Nutr. 2019 Jun;22(8):1351-1360. doi: 10.1017/S1368980019000168. Epub 2019 Feb 26.

PMID:
30803461
40.

Okamoto syndrome has features overlapping with Au-Kline syndrome and is caused by HNRNPK mutation.

Okamoto N.

Am J Med Genet A. 2019 May;179(5):822-826. doi: 10.1002/ajmg.a.61079. Epub 2019 Feb 21.

PMID:
30793470
41.

RALA mutation in a patient with autism spectrum disorder and Noonan syndrome-like phenotype.

Okamoto N, Takata A, Miyake N, Matsumoto N.

Congenit Anom (Kyoto). 2019 Nov;59(6):195-196. doi: 10.1111/cga.12327. Epub 2019 Mar 8. No abstract available.

PMID:
30761613
42.

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome.

van der Sluijs PJ, Jansen S, Vergano SA, Adachi-Fukuda M, Alanay Y, AlKindy A, Baban A, Bayat A, Beck-Wödl S, Berry K, Bijlsma EK, Bok LA, Brouwer AFJ, van der Burgt I, Campeau PM, Canham N, Chrzanowska K, Chu YWY, Chung BHY, Dahan K, De Rademaeker M, Destree A, Dudding-Byth T, Earl R, Elcioglu N, Elias ER, Fagerberg C, Gardham A, Gener B, Gerkes EH, Grasshoff U, van Haeringen A, Heitink KR, Herkert JC, den Hollander NS, Horn D, Hunt D, Kant SG, Kato M, Kayserili H, Kersseboom R, Kilic E, Krajewska-Walasek M, Lammers K, Laulund LW, Lederer D, Lees M, López-González V, Maas S, Mancini GMS, Marcelis C, Martinez F, Maystadt I, McGuire M, McKee S, Mehta S, Metcalfe K, Milunsky J, Mizuno S, Moeschler JB, Netzer C, Ockeloen CW, Oehl-Jaschkowitz B, Okamoto N, Olminkhof SNM, Orellana C, Pasquier L, Pottinger C, Riehmer V, Robertson SP, Roifman M, Rooryck C, Ropers FG, Rosello M, Ruivenkamp CAL, Sagiroglu MS, Sallevelt SCEH, Calvo AS, Simsek-Kiper PO, Soares G, Solaeche L, Sonmez FM, Splitt M, Steenbeek D, Stegmann APA, Stumpel CTRM, Tanabe S, Uctepe E, Utine GE, Veenstra-Knol HE, Venkateswaran S, Vilain C, Vincent-Delorme C, Vulto-van Silfhout AT, Wheeler P, Wilson GN, Wilson LC, Wollnik B, Kosho T, Wieczorek D, Eichler E, Pfundt R, de Vries BBA, Clayton-Smith J, Santen GWE.

Genet Med. 2019 Sep;21(9):2160-2161. doi: 10.1038/s41436-018-0368-y.

43.

Case of multiple disseminated cutaneous lobular capillary hemangioma that developed while taking oral contraceptive pills.

Usui S, Kogame T, Shibuya M, Okamoto N, Toichi E.

J Dermatol. 2019 Jun;46(6):e202-e203. doi: 10.1111/1346-8138.14762. Epub 2019 Jan 10. No abstract available.

PMID:
30628110
44.

Hyperglycemic status is associated with an elevated risk of osteoporotic fracture in community-dwelling elderly Japanese men: The Fujiwara-kyo osteoporosis risk in men (FORMEN) cohort study.

Iki M, Fujita Y, Kouda K, Yura A, Tachiki T, Tamaki J, Sato Y, Moon JS, Hamada M, Kajita E, Okamoto N, Kurumatani N.

Bone. 2019 Apr;121:100-106. doi: 10.1016/j.bone.2019.01.005. Epub 2019 Jan 5.

PMID:
30620891
45.

[Effect of Methylcellulose (Cellulose Derivatives) on Ibuprofen-crushing Efficiency in Nano Pulverizer NP-100].

Nagai N, Yamasaki Y, Nakamura T, Otake H, Okamoto N.

Yakugaku Zasshi. 2019;139(1):123-130. doi: 10.1248/yakushi.18-00176. Japanese.

46.

MYCN de novo gain-of-function mutation in a patient with a novel megalencephaly syndrome.

Kato K, Miya F, Hamada N, Negishi Y, Narumi-Kishimoto Y, Ozawa H, Ito H, Hori I, Hattori A, Okamoto N, Kato M, Tsunoda T, Kanemura Y, Kosaki K, Takahashi Y, Nagata KI, Saitoh S.

J Med Genet. 2019 Jun;56(6):388-395. doi: 10.1136/jmedgenet-2018-105487. Epub 2018 Dec 20.

PMID:
30573562
47.

Heterosis extends the reproductive ability in aged female mice†.

Ozawa Y, Watanabe K, Toda T, Shibuya S, Okumura N, Okamoto N, Sato Y, Kawashima I, Kawamura K, Shimizu T.

Biol Reprod. 2019 Apr 1;100(4):1082-1089. doi: 10.1093/biolre/ioy260.

PMID:
30561512
48.

De novo 1p35.2 microdeletion including PUM1 identified in a patient with sporadic West syndrome.

Imaizumi T, Mogami Y, Okamoto N, Yamamoto-Shimojima K, Yamamoto T.

Congenit Anom (Kyoto). 2019 Nov;59(6):193-194. doi: 10.1111/cga.12322. Epub 2019 Jan 2. No abstract available.

PMID:
30536491
49.

Kabuki syndrome: international consensus diagnostic criteria.

Adam MP, Banka S, Bjornsson HT, Bodamer O, Chudley AE, Harris J, Kawame H, Lanpher BC, Lindsley AW, Merla G, Miyake N, Okamoto N, Stumpel CT, Niikawa N; Kabuki Syndrome Medical Advisory Board.

J Med Genet. 2019 Feb;56(2):89-95. doi: 10.1136/jmedgenet-2018-105625. Epub 2018 Dec 4.

PMID:
30514738
50.

Predictors of side branch compromise in calcified bifurcation lesions treated with orbital atherectomy.

Barman N, Okamoto N, Ueda H, Chamaria S, Bhatheja S, Vengrenyuk Y, Gupta E, Sweeny J, Kapur V, Hasan C, Baber U, Moreno P, Sharma S, Kini AS.

Catheter Cardiovasc Interv. 2019 Jul 1;94(1):45-52. doi: 10.1002/ccd.27992. Epub 2018 Dec 3.

PMID:
30511359

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