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Items: 1 to 50 of 129

1.

Dietary Intake of Ascorbic Acid Attenuates Lipopolysaccharide-Induced Sepsis and Septic Inflammation in ODS Rats.

Kawade N, Tokuda Y, Tsujino S, Aoyama H, Kobayashi M, Murai A, Horio F.

J Nutr Sci Vitaminol (Tokyo). 2018;64(6):404-411. doi: 10.3177/jnsv.64.404.

2.

Unstable Osteochondritis Dissecans of the Glenoid Fixed with Autogenous Osteochondral Plugs in a College Baseball Player: A Case Report.

Tsujino S, Tsujino M, Tsujino A.

JBJS Case Connect. 2018 Oct-Dec;8(4):e99. doi: 10.2106/JBJS.CC.18.00105.

PMID:
30540608
3.

Tenosynovial giant cell tumour of the hand in children under 10 years of age.

Tsujino S, Matsumoto S, Ae K.

J Hand Surg Eur Vol. 2018 Mar;43(3):335-337. doi: 10.1177/1753193417739518. Epub 2017 Nov 6. No abstract available.

PMID:
29105587
4.

Erratum: Measurement of transverse emittance and coherence of double-gate field emitter array cathodes.

Tsujino S, Das Kanungo P, Monshipouri M, Lee C, Dwayne Miller RJ.

Nat Commun. 2017 Feb 24;8:14526. doi: 10.1038/ncomms14526. No abstract available.

5.
6.

Measurement of transverse emittance and coherence of double-gate field emitter array cathodes.

Tsujino S, Das Kanungo P, Monshipouri M, Lee C, Miller RJ.

Nat Commun. 2016 Dec 23;7:13976. doi: 10.1038/ncomms13976.

7.

Ultrasonic acoustic levitation for fast frame rate X-ray protein crystallography at room temperature.

Tsujino S, Tomizaki T.

Sci Rep. 2016 May 6;6:25558. doi: 10.1038/srep25558.

8.

High-density metallic nano-emitter arrays and their field emission characteristics.

Mustonen A, Guzenko V, Spreu C, Feurer T, Tsujino S.

Nanotechnology. 2014 Feb 28;25(8):085203. doi: 10.1088/0957-4484/25/8/085203. Epub 2014 Feb 4.

PMID:
24492288
9.

Efficient light coupling for optically excited high-density metallic nanotip arrays.

Mustonen A, Beaud P, Kirk E, Feurer T, Tsujino S.

Sci Rep. 2012;2:915. doi: 10.1038/srep00915. Epub 2012 Dec 3.

10.

Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosis.

Yoshida T, Sasaki M, Yoshida M, Namekawa M, Okamoto Y, Tsujino S, Sasayama H, Mizuta I, Nakagawa M; Alexander Disease Study Group in Japan.

J Neurol. 2011 Nov;258(11):1998-2008. doi: 10.1007/s00415-011-6056-3. Epub 2011 May 1.

PMID:
21533827
11.

Biochemical and structural study on a S529V mutant acid α-glucosidase responsive to pharmacological chaperones.

Tajima Y, Saito S, Ohno K, Tsukimura T, Tsujino S, Sakuraba H.

J Hum Genet. 2011 Jun;56(6):440-6. doi: 10.1038/jhg.2011.36. Epub 2011 Apr 7.

PMID:
21471980
12.

Novel deletion mutation in GFAP gene in an infantile form of Alexander disease.

Murakami N, Tsuchiya T, Kanazawa N, Tsujino S, Nagai T.

Pediatr Neurol. 2008 Jan;38(1):50-2.

PMID:
18054694
13.

Monovalent Gb3-/Gb2-derivatives conjugated with a phosphatidyl residue: a novel class of Shiga toxin-neutralizing agent.

Neri P, Tokoro S, Yokoyama S, Miura T, Murata T, Nishida Y, Kajimoto T, Tsujino S, Inazu T, Usui T, Mori H.

Biol Pharm Bull. 2007 Sep;30(9):1697-701.

14.

Structural and biochemical studies on Pompe disease and a "pseudodeficiency of acid alpha-glucosidase".

Tajima Y, Matsuzawa F, Aikawa S, Okumiya T, Yoshimizu M, Tsukimura T, Ikekita M, Tsujino S, Tsuji A, Edmunds T, Sakuraba H.

J Hum Genet. 2007;52(11):898-906. Epub 2007 Sep 6.

PMID:
17805474
15.

A case of infantile Alexander disease diagnosed by magnetic resonance imaging and genetic analysis.

Sakakibara T, Takahashi Y, Fukuda K, Inoue T, Kurosawa T, Nishikubo T, Shima M, Taoka T, Aida N, Tsujino S, Kanazawa N, Yoshioka A.

Brain Dev. 2007 Sep;29(8):525-8. Epub 2007 Mar 23.

PMID:
17383133
16.

MR imaging and 1H-MR spectroscopy of a case of van der Knaap disease.

Morita H, Imamura A, Matsuo N, Tatebayashi K, Omoya K, Takahashi Y, Tsujino S.

Brain Dev. 2006 Aug;28(7):466-9. Epub 2006 Feb 28.

PMID:
16504440
17.

A novel R275X mutation of the SLC25A15 gene in a Japanese patient with the HHH syndrome.

Torisu H, Kira R, Kanazawa N, Takemoto M, Sanefuji M, Sakai Y, Tsujino S, Hara T.

Brain Dev. 2006 Jun;28(5):332-5. Epub 2006 Jan 10.

PMID:
16376511
18.

Benign course of glycogen storage disease type IIb in two brothers: nature or nurture?

Slonim AE, Bulone L, Minikes J, Hays AP, Shanske S, Tsujino S, DiMauro S.

Muscle Nerve. 2006 Apr;33(4):571-4.

PMID:
16320310
19.

An infantile-juvenile form of Alexander disease caused by a R79H mutation in GFAP.

Asahina N, Okamoto T, Sudo A, Kanazawa N, Tsujino S, Saitoh S.

Brain Dev. 2006 Mar;28(2):131-3. Epub 2005 Sep 15.

20.

In vivo alemtuzumab enables haploidentical human leukocyte antigen-mismatched hematopoietic stem-cell transplantation without ex vivo graft manipulation.

Kanda Y, Oshima K, Asano-Mori Y, Kandabashi K, Nakagawa M, Sakata-Yanagimoto M, Izutsu K, Hangaishi A, Tsujino S, Ogawa S, Motokura T, Chiba S, Hirai H.

Transplantation. 2005 May 27;79(10):1351-7.

PMID:
15912103
21.

[Glial fibrillary acidic protein mutation in a Chinese girl with infantile Alexander disease].

Ma HW, Lu JF, Jiang J, Chen LY, Niu GH, Wu BM, Kanazawa N, Tsujino S.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Feb;22(1):79-81. Chinese.

PMID:
15696488
22.

[A case of long-term survival of a patient with infantile Alexander disease diagnosed by DNA analysis].

Wakabayashi K, Lai M, Masuko K, Yamashita S, Yamada M, Iwamoto H, Aida N, Shiroma N, Kanazawa N, Tsujino S.

No To Hattatsu. 2005 Jan;37(1):55-9. Review. Japanese.

PMID:
15675360
23.

Clinical significance of peripheral blood erythroblastosis after hematopoietic stem cell transplantation.

Goyama S, Kanda Y, Nannya Y, Ogawa S, Asano-Moki Y, Ogawa N, Nakagawa M, Sakata-Yanagimoto M, Kawazu M, Komeno Y, Imai Y, Hangaishi A, Kurokawa M, Tsujino S, Aoki K, Chiba S, Motokura T, Hirai H.

Leuk Lymphoma. 2004 Dec;45(12):2439-43.

PMID:
15621756
24.

Predictors for severe cardiac complications after hematopoietic stem cell transplantation.

Sakata-Yanagimoto M, Kanda Y, Nakagawa M, Asano-Mori Y, Kandabashi K, Izutsu K, Imai Y, Hangaishi A, Kurokawa M, Tsujino S, Ogawa S, Chiba S, Motokura T, Hirai H.

Bone Marrow Transplant. 2004 May;33(10):1043-7.

PMID:
15064691
25.

A case of infantile Alexander disease with a milder phenotype and a novel GFAP mutation, L90P.

Suzuki Y, Kanazawa N, Takenaka J, Okumura A, Negoro T, Tsujino S.

Brain Dev. 2004 Apr;26(3):206-8.

PMID:
15030911
26.
27.

Increased incidence of acute graft-versus-host disease with the continuous infusion of cyclosporine A compared to twice-daily infusion.

Ogawa N, Kanda Y, Matsubara M, Asano Y, Nakagawa M, Sakata-Yanagimoto M, Kandabashi K, Izutsu K, Imai Y, Hangaishi A, Kurokawa M, Tsujino S, Ogawa S, Aoki K, Chiba S, Motokura T, Hirai H.

Bone Marrow Transplant. 2004 Mar;33(5):549-52.

PMID:
14716350
28.

Ischemic colitis as a manifestation of thrombotic microangiopathy following bone marrow transplantation.

Komeno Y, Ogawa S, Ishida T, Takeuchi K, Tsujino S, Kurokawa M, Aoki K, Kanda Y, Chiba S, Motokura T, Fukayama M, Hirai H.

Intern Med. 2003 Dec;42(12):1228-32.

29.

Male predominance among Japanese adult patients with late-onset hemorrhagic cystitis after hematopoietic stem cell transplantation.

Asano Y, Kanda Y, Ogawa N, Sakata-Yanagimoto M, Nakagawa M, Kawazu M, Goyama S, Kandabashi K, Izutsu K, Imai Y, Hangaishi A, Kurokawa M, Tsujino S, Ogawa S, Aoki K, Chiba S, Motokura T, Hirai H.

Bone Marrow Transplant. 2003 Dec;32(12):1175-9. Review.

PMID:
14647272
30.

New GAA mutations in Japanese patients with GSDII (Pompe disease).

Pipo JR, Feng JH, Yamamoto T, Ohsaki Y, Nanba E, Tsujino S, Sakuragawa N, Martiniuk F, Ninomiya H, Oka A, Ohno K.

Pediatr Neurol. 2003 Oct;29(4):284-7.

PMID:
14643388
31.

A common mutation and a novel mutation in Japanese patients with van der Knaap disease.

Tsujino S, Kanazawa N, Yoneyama H, Shimono M, Kawakami A, Hatanaka Y, Shimizu T, Oba H.

J Hum Genet. 2003;48(12):605-8. Epub 2003 Nov 13.

PMID:
14615938
32.

Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genes.

Mancuso M, Filosto M, Tsujino S, Lamperti C, Shanske S, Coquet M, Desnuelle C, DiMauro S.

Arch Neurol. 2003 Oct;60(10):1445-7. Erratum in: Arch Neurol. 2004 Jan;61(1):29.

PMID:
14568816
33.

A case of megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap disease): molecular genetic study.

Saijo H, Nakayama H, Ezoe T, Araki K, Sone S, Hamaguchi H, Suzuki H, Shiroma N, Kanazawa N, Tsujino S, Hirayama Y, Arima M.

Brain Dev. 2003 Aug;25(5):362-6.

PMID:
12850517
34.

Reduced-intensity bone marrow transplantation from an alternative unrelated donor for myelodysplastic syndrome of first-donor origin.

Komeno Y, Kanda Y, Kandabashi K, Kawazu M, Goyama S, Takeshita M, Nannya Y, Niino M, Nakamoto T, Kurokawa M, Tsujino S, Ogawa S, Aoki K, Chiba S, Motokura T, Hirai H.

Am J Hematol. 2003 Mar;72(3):220-2.

35.

Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L.

Shiroma N, Kanazawa N, Kato Z, Shimozawa N, Imamura A, Ito M, Ohtani K, Oka A, Wakabayashi K, Iai M, Sugai K, Sasaki M, Kaga M, Ohta T, Tsujino S.

Brain Dev. 2003 Mar;25(2):116-21.

PMID:
12581808
36.

Reverse seroconversion of hepatitis B virus after hematopoietic stem cell transplantation.

Goyama S, Kanda Y, Nannya Y, Kawazu M, Takeshita M, Niino M, Komeno Y, Nakamoto T, Kurokawa M, Tsujino S, Ogawa S, Aoki K, Chiba S, Motokura T, Shiratori Y, Hirai H.

Leuk Lymphoma. 2002 Nov;43(11):2159-63. Review.

PMID:
12533042
37.

Rapid diagnosis of invasive pulmonary aspergillosis by quantitative polymerase chain reaction using bronchial lavage fluid.

Kawazu M, Kanda Y, Goyama S, Takeshita M, Nannya Y, Niino M, Komeno Y, Nakamoto T, Kurokawa M, Tsujino S, Ogawa S, Aoki K, Chiba S, Motokura T, Ohishi N, Hirai H.

Am J Hematol. 2003 Jan;72(1):27-30.

38.

Amelioration of prolidase deficiency in fibroblasts using adenovirus mediated gene transfer.

Ikeda K, Tohyama J, Tsujino S, Sato K, Oono T, Arata J, Endo F, Sakuragawa N.

Jpn J Hum Genet. 1997 Sep;42(3):401-8.

PMID:
12503186
39.

[Metabolic disorder of carbohydrate].

Shiroma N, Tsujino S.

Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):152-5. Review. Japanese. No abstract available.

PMID:
12483851
40.
41.

[Mitochondrial ornithine transporter deficiency].

Tsujino S, Miyamoto T, Kanazawa N.

Nihon Rinsho. 2002 Apr;60 Suppl 4:779-82. Review. Japanese. No abstract available.

PMID:
12013998
42.

A novel mutation, P126R, in a Japanese patient with HHH syndrome.

Miyamoto T, Kanazawa N, Hayakawa C, Tsujino S.

Pediatr Neurol. 2002 Jan;26(1):65-7.

PMID:
11814739
43.

[Adult form of acid maltase deficiency presenting with pattern of muscle weakness resembling facioscapulohumeral dystrophy].

Oya Y, Morita H, Ogawa M, Nonaka I, Tsujino S, Kawai M.

Rinsho Shinkeigaku. 2001 Jul;41(7):390-6. Japanese.

PMID:
11808348
44.

[Molecular genetic studies of mitochondrial ornithine transporter deficiency (HHH syndrome)].

Tsujino S, Miyamoto T, Kanazawa N.

Nihon Rinsho. 2001 Nov;59(11):2278-84. Review. Japanese.

PMID:
11712419
45.

[Acid maltase deficiency].

Miyamoto T, Tsujino S.

Ryoikibetsu Shokogun Shirizu. 2001;(36):8-13. Review. Japanese. No abstract available.

PMID:
11596457
46.

[Disorders of carbohydrate metabolism (glycogenoses): an overview].

Tsujino S.

Ryoikibetsu Shokogun Shirizu. 2001;(36):5-7. Review. Japanese. No abstract available.

PMID:
11596447
47.

[Muscle phosphoglycerate mutase deficiency].

Tsujino S.

Ryoikibetsu Shokogun Shirizu. 2001;(36):41-2. Review. Japanese. No abstract available.

PMID:
11596425
48.

[Aldolase A deficiency].

Tsujino S.

Ryoikibetsu Shokogun Shirizu. 2001;(36):35-6. Review. Japanese. No abstract available.

PMID:
11596407
49.

[Glycogen branching enzyme deficiency (Andersen disease)].

Tsujino S.

Ryoikibetsu Shokogun Shirizu. 2001;(36):23-4. Review. Japanese. No abstract available.

PMID:
11596376
50.

[Glycogen debranching enzyme deficiency (Forbes-Cori disease)].

Tsujino S.

Ryoikibetsu Shokogun Shirizu. 2001;(36):20-2. Review. Japanese. No abstract available.

PMID:
11596370

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