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A case of acute encephalophathy with residual neurological sequelae induced by immunoglobulin A vasculitis

Hamano, H., Matsushige, T., Inoue, H., Hoshide, M., Kobayashi, H., Kohno, F., Oka, M., Ichiyama, T., Ohga, S., Ouchi, K. & Hasegawa, S., Sep 2019, In : Journal of Clinical Neuroscience. 67, p. 270-271 2 p.

Research output: Contribution to journalArticle

Vasculitis
Immunoglobulin A
Brain Diseases
Cerebrovascular Circulation
Cerebrospinal Fluid

A child with prostaglandin I2-associated thyrotoxicosis: Case report

Sonoda, Y., Yamamura, K., Ishii, K., Ohkubo, K., Ihara, K., Sakai, Y. & Ohga, S., Jun 2019, In : JCRPE Journal of Clinical Research in Pediatric Endocrinology. 11, 2, p. 207-210 4 p.

Research output: Contribution to journalArticle

Open Access
Thyrotoxicosis
Epoprostenol
Hyperthyroidism
Pulmonary Hypertension
Thyroid Gland
3 Citations (Scopus)

Acute pericardial effusion representing the tnf-α-mediated severe inflammation but not the coronary artery outcome of Kawasaki disease

Okada, S., Hasegawa, S., Suzuki, Y., Matsubara, T., Shimomura, M., Okuda, M., Ichiyama, T. & Ohga, S., May 1 2015, In : Scandinavian Journal of Rheumatology. 44, 3, p. 247-252 6 p.

Research output: Contribution to journalArticle

Mucocutaneous Lymph Node Syndrome
Pericardial Effusion
Coronary Vessels
Inflammation
Tumor Necrosis Factor Receptors
3 Citations (Scopus)

Adjunct cyclosporine therapy for refractory Kawasaki disease in a very young infant

Okada, S., Azuma, Y., Suzuki, Y., Yamada, H., Wakabayashi-Takahara, M., Korenaga, Y., Akase, H., Hasegawa, S. & Ohga, S., Apr 1 2016, In : Pediatrics International. 58, 4, p. 295-298 4 p.

Research output: Contribution to journalArticle

Mucocutaneous Lymph Node Syndrome
Cyclosporine
Immunoglobulins
Coronary Vessels
Therapeutics

Adjuvant recombinant thrombomodulin therapy for hepatopathy induced by vincristine, actinomycin D, and cyclophosphamide in pediatric rhabdomyosarcoma: A case report

Kobayashi, T., Noguchi, M., Nakayama, H., Fukano, R. & Ohga, S., Jan 1 2019, In : Molecular and Clinical Oncology. 11, 2, p. 208-212 5 p.

Research output: Contribution to journalArticle

Thrombomodulin
Rhabdomyosarcoma
Dactinomycin
Vincristine
Cyclophosphamide
4 Citations (Scopus)

Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism

Ichiyama, M., Ohga, S., Ochiai, M., Tanaka, K., Matsunaga, Y., Kusuda, T., Inoue, H., Ishimura, M., Takimoto, T., Koga, Y., Hotta, T., Kang, D. & Hara, T., Jan 1 2016, In : Pediatric Research. 79, 1, p. 81-86 6 p.

Research output: Contribution to journalArticle

Thromboembolism
Age Distribution
Age of Onset
Anticoagulants
Pediatrics
3 Citations (Scopus)

A male case with CDKL5-associated encephalopathy manifesting transient methylmalonic acidemia

Akamine, S., Ishizaki, Y., Sakai, Y., Torisu, H., Fukai, R., Miyake, N., Ohkubo, K., Koga, H., Sanefuji, M., Sakata, A., Kimura, M., Yamaguchi, S., Sakamoto, O., Hara, T., Saitsu, H., Matsumoto, N. & Ohga, S., Aug 2018, In : European Journal of Medical Genetics. 61, 8, p. 451-454 4 p.

Research output: Contribution to journalArticle

Brain Diseases
Mutation
Methylmalonic Acid
Exome
Infantile Spasms

An acute encephalopathy with reduced diffusion in BRAF-associated cardio-facio-cutaneous syndrome

Okuzono, S., Fukai, R., Noda, M., Miyake, N., Lee, S., Kaku, N., Sanefuji, M., Akamine, S., Kanno, S., Ishizaki, Y., Torisu, H., Kira, R., Matsumoto, N., Sakai, Y. & Ohga, S., Apr 2019, In : Brain and Development. 41, 4, p. 378-381 4 p.

Research output: Contribution to journalArticle

Brain Diseases
Exome
Mutation
Inborn Genetic Diseases
Sick Leave
7 Citations (Scopus)

A nationwide survey of common viral infections in childhood among patients with primary immunodeficiency diseases

Nanishi, E., Hoshina, T., Takada, H., Ishimura, M., Nishio, H., Uehara, T., Mizuno, Y., Hasegawa, S., Ohga, S., Nagao, M., Igarashi, M., Yajima, S., Kusumoto, Y., Onishi, N., Sasahara, Y., Yasumi, T., Heike, T., Hara, T., Kobayashi, C., Ishige, T. & 30 others, Kudo, K., Suzuki, K., Ogata, S., Kikuchi, M., Kurihara, Y., Niiya, R., Katsuta, T., Saikawa, Y., Yoshida, H., Ishizaki, Y., Hayakawa, A., Shirakawa, T., Mori, T., Suzuki, Y., Tsuda, H., Sato, T., Waragai, T., Kumaki, S., Komiyama, O., Seto, M., Kadoya, R., Ohbuchi, N., Kozan, H., Shimizu, H., Imagawa, T., Yamada, Y., Hara, T., Ohno, T., Ota, E. & Toda, H., Oct 1 2016, In : Journal of Infection. 73, 4, p. 358-368 11 p.

Research output: Contribution to journalArticle

Virus Diseases
Rotavirus Infections
Respiratory Syncytial Virus Infections
Orthomyxoviridae
Japan
18 Citations (Scopus)

A nationwide survey of opsoclonus-myoclonus syndrome in Japanese children

Japanese Society for Pediatric Immune-mediated Brain Diseases, Aug 1 2015, In : Brain and Development. 37, 7, p. 656-660 5 p.

Research output: Contribution to journalArticle

Opsoclonus-Myoclonus Syndrome
Ocular Motility Disorders
Therapeutics
Surveys and Questionnaires
Myoclonus

A nationwide survey on tracheostomy for very-low-birth-weight infants in Japan

on behalf of the Neonatal Research Network of Japan, Jan 2019, In : Pediatric Pulmonology. 54, 1, p. 53-60 8 p.

Research output: Contribution to journalArticle

Very Low Birth Weight Infant
Tracheostomy
Japan
Odds Ratio
Parturition

A rightward saccade to an unexpected stimulus as a marker for lateralised visuospatial attention /631/378/2649/1310 /631/378/2617/1795 /631/477/2811 article

Sanefuji, M., Yamashita, H., Torio, M., Katsuki, D., Akamine, S., Ishizaki, Y., Kishimoto, J., Sakai, Y., Takada, H., Yoshida, K. & Ohga, S., Dec 1 2018, In : Scientific reports. 8, 1, 7562.

Research output: Contribution to journalArticle

Saccades
Reaction Time
Task Performance and Analysis
Healthy Volunteers
Brain

Association of perinatal factors of epilepsy in very low birth weight infants, using a nationwide database in Japan

on behalf of the Neonatal Research Network of Japan (NRNJ), Nov 1 2019, In : Journal of Perinatology. 39, 11, p. 1472-1479 8 p.

Research output: Contribution to journalArticle

Open Access
Very Low Birth Weight Infant
Epilepsy
Japan
Databases
Odds Ratio

A survey on the status of countermeasures against anticancer drug exposure for families-focus on pediatric cancer hospitals

Ohta, M., Noda, Y., Miyazono, M., Koga, Y., Kifune, M., Hamada, M., Taguchi, T. & Ohga, S., Apr 2019, In : Japanese Journal of Cancer and Chemotherapy. 46, 4, p. 673-677 5 p.

Research output: Contribution to journalArticle

Cancer Care Facilities
Pediatric Hospitals
Pharmaceutical Preparations
Occupational Exposure
Nurses
21 Citations (Scopus)

ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia

Arashiki, N., Takakuwa, Y., Mohandas, N., Hale, J., Yoshida, K., Ogura, H., Utsugisawa, T., Ohga, S., Miyano, S., Ogawa, S., Kojima, S. & Kanno, H., Apr 30 2016, In : Haematologica. 101, 5, p. 559-565 7 p.

Research output: Contribution to journalArticle

Congenital Hemolytic Anemia
Phosphatidylserines
Erythrocytes
Erythrocyte Aging
X-Linked Genes
2 Citations (Scopus)

Atypical erythroblastosis in a patient with Diamond–Blackfan anemia who developed del(20q) myelodysplasia

Sonoda, M., Ishimura, M., Ichimiya, Y., Terashi, E., Eguchi, K., Sakai, Y., Takada, H., Hama, A., Kanno, H., Toki, T., Ito, E. & Ohga, S., Aug 1 2018, In : International journal of hematology. 108, 2, p. 228-231 4 p.

Research output: Contribution to journalArticle

Anemia
Neonatal Anemia
Clonal Evolution
Chelation Therapy
Refractory Anemia
4 Citations (Scopus)

Blood reference intervals for preterm low-birth-weight infants: A multicenter cohort study in Japan

Ochiai, M., Matsushita, Y., Inoue, H., Kusuda, T., Kang, D., Ichihara, K., Nakashima, N., Ihara, K., Ohga, S. & Hara, T., Aug 2016, In : PloS one. 11, 8, e0161439.

Research output: Contribution to journalArticle

low birth weight
gestational age
Premature Birth
Low Birth Weight Infant
cohort studies
2 Citations (Scopus)

Burden of Human Metapneumovirus and Respiratory Syncytial Virus Infections in Asthmatic Children

Furuta, T., Hasegawa, S., Mizutani, M., Iwai, T., Ohbuchi, N., Kawano, S., Tashiro, N., Uchida, M., Hasegawa, M., Motoyama, M., Sekino, T., Nakatsuka, K., Ichihara, K., Shirabe, K. & Ohga, S., Nov 1 2018, In : The Pediatric infectious disease journal. 37, 11, p. 1107-1111 5 p.

Research output: Contribution to journalArticle

Human respiratory syncytial virus
Metapneumovirus
Respiratory Syncytial Virus Infections
Infection
Odds Ratio
2 Citations (Scopus)

Cancer management in kabuki syndrome: The first case of wilms tumor and a literature review

Teranishi, H., Koga, Y., Nakashima, K., Morihana, E., Ishii, K., Sakai, Y., Taguchi, T., Oda, Y., Miyake, N., Matsumoto, N. & Ohga, S., Jul 1 2018, In : Journal of Pediatric Hematology/Oncology. 40, 5, p. 391-394 4 p.

Research output: Contribution to journalArticle

Wilms Tumor
Neoplasms
Dandy-Walker Syndrome
Hypoplastic Left Heart Syndrome
Mutation
6 Citations (Scopus)

Cat-scratch disease with severe pleuritis in a 6-year-old girl

Kimura, S., Hasegawa, S., Yanagihara, M., Inoue, H., Matsushige, T., Tsuneoka, H., Ichiyama, T. & Ohga, S., Jun 1 2015, In : Pediatrics International. 57, 3, p. 501-503 3 p.

Research output: Contribution to journalArticle

Cat-Scratch Disease
Pleurisy
Real-Time Polymerase Chain Reaction
Bartonella henselae
Lymphadenitis

Chemokine levels predict progressive liver disease in Down syndrome patients with transient abnormal myelopoiesis

Kinjo, T., Inoue, H., Kusuda, T., Fujiyoshi, J., Ochiai, M., Takahata, Y., Honjo, S., Koga, Y., Hara, T. & Ohga, S., Aug 2019, In : Pediatrics and Neonatology. 60, 4, p. 382-388 7 p.

Research output: Contribution to journalArticle

Down Syndrome
Chemokines
Liver Failure
Liver Diseases
Chemokine CXCL9

Circulating endothelial glycocalyx components as a predictive marker of coronary artery lesions in Kawasaki disease

Ohnishi, Y., Yasudo, H., Suzuki, Y., Furuta, T., Matsuguma, C., Azuma, Y., Miyake, A., Okada, S., Ichihara, K., Ohga, S. & Hasegawa, S., Oct 1 2019, In : International Journal of Cardiology. 292, p. 236-240 5 p.

Research output: Contribution to journalArticle

Glycocalyx
Mucocutaneous Lymph Node Syndrome
Syndecan-1
Coronary Vessels
Hyaluronic Acid

Clinical Features, Molecular Genetics, and Long-Term Outcome in Congenital Chloride Diarrhea: A Nationwide Study in Japan

Konishi, K. I., Mizuochi, T., Yanagi, T., Watanabe, Y., Ohkubo, K., Ohga, S., Maruyama, H., Takeuchi, I., Sekine, Y., Masuda, K., Kikuchi, N., Yotsumoto, Y., Ohtsuka, Y., Tanaka, H., Kudo, T., Noguchi, A., Fuwa, K., Mushiake, S., Ida, S., Fujishiro, J. & 3 others, Yamashita, Y., Taguchi, T. & Yamamoto, K., Nov 2019, In : Journal of Pediatrics. 214, p. 151-157.e6

Research output: Contribution to journalArticle

Molecular Biology
Japan
Mutation
Far East
Congenital chloride diarrhea

Clinical Utility of Highly Purified 10% Liquid Intravenous Immunoglobulin in Kawasaki Disease

Oda, T., Nagata, H., Nakashima, Y., Nanishi, E., Takada, Y., Nishimura, M., Kubo, E., Hatae, K. & Ohga, S., Nov 2019, In : Journal of Pediatrics. 214, p. 227-230 4 p.

Research output: Contribution to journalArticle

Mucocutaneous Lymph Node Syndrome
Intravenous Immunoglobulins
Fever
Therapeutics
16 Citations (Scopus)

Comparison of long-term outcomes between children with aplastic anemia and refractory cytopenia of childhood who received immunosuppressive therapy with antithymocyte globulin and cyclosporine

Hama, A., Takahashi, Y., Muramatsu, H., Ito, M., Narita, A., Kosaka, Y., Tsuchida, M., Kobayashi, R., Ito, E., Yabe, H., Ohga, S., Ohara, A. & Kojima, S., Oct 31 2015, In : Haematologica. 100, 11, p. 1426-1433 8 p.

Research output: Contribution to journalArticle

Antilymphocyte Serum
Aplastic Anemia
Immunosuppressive Agents
Cyclosporine
Clonal Evolution
1 Citation (Scopus)

Complement activation associated with ADAMTS13 deficiency may contribute to the characteristic glomerular manifestations in Upshaw-Schulman syndrome

Itami, H., Hara, S., Matsumoto, M., Imamura, S., Kanai, R., Nishiyama, K., Ishimura, M., Ohga, S., Yoshida, M., Tanaka, R., Ogawa, Y., Asada, Y., Sekita-Hatakeyama, Y., Hatakeyama, K. & Ohbayashi, C., Oct 2018, In : Thrombosis Research. 170, p. 148-155 8 p.

Research output: Contribution to journalArticle

Thrombotic Thrombocytopenic Purpura
Complement Activation
Complement Membrane Attack Complex
Complement C5b
Staining and Labeling
17 Citations (Scopus)

Coronary artery lesions and the increasing incidence of Kawasaki disease resistant to initial immunoglobulin

Kibata, T., Suzuki, Y., Hasegawa, S., Matsushige, T., Kusuda, T., Hoshide, M., Takahashi, K., Okada, S., Wakiguchi, H., Moriwake, T., Uchida, M., Ohbuchi, N., Iwai, T., Hasegawa, M., Ichihara, K., Yashiro, M., Makino, N., Nakamura, Y. & Ohga, S., Jul 1 2016, In : International Journal of Cardiology. 214, p. 209-215 7 p.

Research output: Contribution to journalArticle

Mucocutaneous Lymph Node Syndrome
Intravenous Immunoglobulins
Immunoglobulins
Coronary Vessels
Adrenal Cortex Hormones

Critical association of Pallister–Hall syndrome and congenital heart disease

Ochiai, M., Nagata, H., Tanaka, K., Ihara, K. & Ohga, S., Jan 1 2019, In : Pediatrics International. 61, 8, p. 827-828 2 p.

Research output: Contribution to journalArticle

Pallister-Hall Syndrome
Heart Diseases

Decision-making dilemmas of paediatricians: A qualitative study in Japan

Sasazuki, M., Sakai, Y., Kira, R., Toda, N., Ichimiya, Y., Akamine, S., Torio, M., Ishizaki, Y., Sanefuji, M., Narama, M., Itai, K., Hara, T., Takada, H., Kizawa, Y. & Ohga, S., Aug 1 2019, In : BMJ open. 9, 8, e026579.

Research output: Contribution to journalArticle

Open Access
Decision Making
Japan
Interviews
Consensus
Professional Education
3 Citations (Scopus)

De Novo Mutations Activating Germline TP53 in an Inherited Bone-Marrow-Failure Syndrome

Toki, T., Yoshida, K., Wang, R. N., Nakamura, S., Maekawa, T., Goi, K., Katoh, M. C., Mizuno, S., Sugiyama, F., Kanezaki, R., Uechi, T., Nakajima, Y., Sato, Y., Okuno, Y., Sato-Otsubo, A., Shiozawa, Y., Kataoka, K., Shiraishi, Y., Sanada, M., Chiba, K. & 19 others, Tanaka, H., Terui, K., Sato, T., Kamio, T., Sakaguchi, H., Ohga, S., Kuramitsu, M., Hamaguchi, I., Ohara, A., Kanno, H., Miyano, S., Kojima, S., Ishiguro, A., Sugita, K., Kenmochi, N., Takahashi, S., Eto, K., Ogawa, S. & Ito, E., Sep 6 2018, In : American journal of human genetics. 103, 3, p. 440-447 8 p.

Research output: Contribution to journalArticle

Germ-Line Mutation
Dyskeratosis Congenita
Diamond-Blackfan Anemia
Induced Pluripotent Stem Cells
Agammaglobulinemia

De novo p.G696S mutation in COL4A1 causes intracranial calcification and late-onset cerebral hemorrhage: A case report and review of the literature

Kinoshita, K., Ishizaki, Y., Yamamoto, H., Sonoda, M., Yonemoto, K., Kira, R., Sanefuji, M., Ueda, A., Matsui, H., Ando, Y., Sakai, Y. & Ohga, S., Jan 1 2019, (Accepted/In press) In : European Journal of Medical Genetics. 103825.

Research output: Contribution to journalArticle

Cerebral Hemorrhage
Mutation
Exome
Leukoencephalopathies
Collagen Type IV
2 Citations (Scopus)

Diagnostic challenge of the newborn patients with heritable protein C deficiency

Ichiyama, M., Inoue, H., Ochiai, M., Ishimura, M., Shiraishi, A., Fujiyoshi, J., Yamashita, H., Sato, K., Matsumoto, S., Hotta, T., Uchiumi, T., Kang, D. & Ohga, S., Feb 1 2019, In : Journal of Perinatology. 39, 2, p. 212-219 8 p.

Research output: Contribution to journalArticle

Protein C Deficiency
Protein C
Protein S
Newborn Infant
Mutation

Diagnostic potential of stored dried blood spots for inborn errors of metabolism: A metabolic autopsy of medium-chain acyl-CoA dehydrogenase deficiency

Kaku, N., Ihara, K., Hirata, Y., Yamada, K., Lee, S., Kanemasa, H., Motomura, Y., Baba, H., Tanaka, T., Sakai, Y., Maehara, Y. & Ohga, S., Oct 1 2018, In : Journal of Clinical Pathology. 71, 10, p. 885-889 5 p.

Research output: Contribution to journalArticle

Inborn Errors Metabolism
Autopsy
Molecular Biology
Cause of Death
Newborn Infant
5 Citations (Scopus)

Drug reaction with eosinophilia and systemic symptoms during primary Epstein-Barr virus infection

Nanishi, E., Hoshina, T., Ohga, S., Nishio, H. & Hara, T., Feb 1 2015, In : Journal of Microbiology, Immunology and Infection. 48, 1, p. 109-112 4 p.

Research output: Contribution to journalArticle

Drug Hypersensitivity Syndrome
cefditoren pivoxil
Epstein-Barr Virus Infections
Lymphocyte Activation
Human Herpesvirus 4

Dynamics of immunocyte activation during intravenous immunoglobulin treatment in Kawasaki disease

Matsuguma, C., Wakiguchi, H., Suzuki, Y., Okada, S., Furuta, T., Ohnishi, Y., Azuma, Y., Ohga, S. & Hasegawa, S., Nov 2 2019, In : Scandinavian Journal of Rheumatology. 48, 6, p. 491-496 6 p.

Research output: Contribution to journalArticle

Mucocutaneous Lymph Node Syndrome
Intravenous Immunoglobulins
Therapeutics
HLA Antigens
T-Lymphocytes
1 Citation (Scopus)

Early canakinumab therapy for the sensorineural deafness in a family with Muckle-Wells syndrome due to a novel mutation of NLRP3 gene

Iida, Y., Wakiguchi, H., Okazaki, F., Nakamura, T., Yasudo, H., Kubo, M., Sugahara, K., Yamashita, H., Suehiro, Y., Okayama, N., Hashimoto, K., Iwamoto, N., Kawakami, A., Aoki, Y., Takada, H., Ohga, S. & Hasegawa, S., Mar 14 2019, In : Clinical Rheumatology. 38, 3, p. 943-948 6 p.

Research output: Contribution to journalArticle

Cryopyrin-Associated Periodic Syndromes
Deafness
Secondary Prevention
Mutation
Genes

Early Intervention With Adrenocorticotropin for Acute Encephalopathy-Associated Epileptic Spasms: Report of Two Cases

Yonemoto, K., Ichimiya, Y., Sanefuji, M., Kaku, N., Sakata, A., Baba, R., Yamashita, F., Akamine, S., Torio, M., Ishizaki, Y., Maehara, Y., Sakai, Y. & Ohga, S., Jan 1 2019, In : Clinical EEG and Neuroscience. 50, 1, p. 51-55 5 p.

Research output: Contribution to journalArticle

Spasm
Brain Diseases
Adrenocorticotropic Hormone
Electroencephalography
Sick Leave
1 Citation (Scopus)

Early-onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1 and MAGEL2

Akamine, S., Sagata, N., Sakai, Y., Kato, T. A., Nakahara, T., Matsushita, Y., Togao, O., Hiwatashi, A., Sanefuji, M., Ishizaki, Y., Torisu, H., Saitsu, H., Matsumoto, N., Hara, T., Sawa, A., Kano, S., Furue, M., Kanba, S., Shaw, C. A. & Ohga, S., Jan 1 2018, In : Epilepsia Open. 3, 1, p. 81-85 5 p.

Research output: Contribution to journalArticle

Open Access
Neurofibromatosis 1
Brain Diseases
Mutation
Exome
Genes
2 Citations (Scopus)

Effective infliximab therapy for the early regression of coronary artery aneurysm in Kawasaki disease

Nagatomo, Y., Muneuchi, J., Nakashima, Y., Nanishi, E., Shirozu, H., Watanabe, M., Uike, K., Nagata, H., Hirata, Y., Yamamura, K., Takahashi, Y., Okada, S., Suzuki, Y., Hasegawa, S. & Ohga, S., Nov 15 2018, In : International Journal of Cardiology. 271, p. 317-321 5 p.

Research output: Contribution to journalArticle

Coronary Aneurysm
Mucocutaneous Lymph Node Syndrome
Coronary Vessels
Therapeutics
Infliximab
1 Citation (Scopus)

Effective shunt closure for pulmonary hypertension and liver dysfunction in congenital portosystemic venous shunt

Uike, K., Nagata, H., Hirata, Y., Yamamura, K., Terashi, E., Matsuura, T., Morihana, E., Ohkubo, K., Ishii, K., Sakai, Y., Taguchi, T. & Ohga, S., Apr 2018, In : Pediatric Pulmonology. 53, 4, p. 505-511 7 p.

Research output: Contribution to journalArticle

Pulmonary Hypertension
Liver Diseases
Hypertension
Patent Ductus Venosus
Vascular Malformations
2 Citations (Scopus)
Tetralogy of Fallot
Liver Cirrhosis
Carcinoma
Liver
Hyaluronic Acid
1 Citation (Scopus)

Epstein-Barr virus-associated γδ T-cell lymphoproliferative disorder associated with hypomorphic IL2RG mutation

Tanita, K., Hoshino, A., Imadome, K. I., Kamiya, T., Inoue, K., Okano, T., Yeh, T. W., Yanagimachi, M., Shiraishi, A., Ishimura, M., Schober, T., Rohlfs, M., Takagi, M., Imai, K., Takada, H., Ohga, S., Klein, C., Morio, T. & Kanegane, H., Jan 1 2019, In : Frontiers in Pediatrics. 7, FEB, 15.

Research output: Contribution to journalArticle

Open Access
Lymphoproliferative Disorders
Human Herpesvirus 4
T-Lymphocytes
Mutation
Infectious Mononucleosis
5 Citations (Scopus)

Erythrocyte glutathione is a novel biomarker of Diamond-Blackfan anemia

Utsugisawa, T., Uchiyama, T., Toki, T., Ogura, H., Aoki, T., Hamaguchi, I., Ishiguro, A., Ohara, A., Kojima, S., Ohga, S., Ito, E. & Kanno, H., Jul 1 2016, In : Blood Cells, Molecules, and Diseases. 59, p. 31-36 6 p.

Research output: Contribution to journalArticle

Diamond-Blackfan Anemia
Glutathione
Adenosine Deaminase
Erythrocytes
Biomarkers
1 Citation (Scopus)

Factors predicting the recurrence of Epstein–Barr virus-associated hemophagocytic lymphohistiocytosis in children after treatment using the HLH-2004 protocol

Yanagaisawa, R., Matsuda, K., Ohga, S., Kanegane, H., Morimoto, A., Okamoto, Y., Ohara, A., Fukushima, K., Sotomatsu, M., Nomura, K., Saito, A. M., Horibe, K., Ishii, E. & Nakazawa, Y., May 3 2019, In : International journal of hematology. 109, 5, p. 612-617 6 p.

Research output: Contribution to journalArticle

Hemophagocytic Lymphohistiocytosis
Viruses
Recurrence
T-Cell Antigen Receptor
Therapeutics
7 Citations (Scopus)

Fetal hydrocephalus and neonatal stroke as the first presentation of protein C deficiency

Ichiyama, M., Ohga, S., Ochiai, M., Fukushima, K., Ishimura, M., Torio, M., Urata, M., Hotta, T., Kang, D. & Hara, T., Feb 1 2016, In : Brain and Development. 38, 2, p. 253-256 4 p.

Research output: Contribution to journalArticle

Protein C Deficiency
Hydrocephalus
Heterozygote
Stroke
Thromboembolism

Fever and skin involvement at diagnosis predicting the intractable langerhans cell histiocytosis: 40 case-series in a single center

Kobayashi, T., Koga, Y., Ishimura, M., Nakashima, K., Kato, W., Ono, H., Sonoda, M., Eguchi, K., Fukano, R., Honjo, S., Oda, Y. & Ohga, S., Jan 1 2018, In : Journal of Pediatric Hematology/Oncology. 40, 3, p. e148-e153

Research output: Contribution to journalArticle

Langerhans Cell Histiocytosis
Fever
Skin
Confidence Intervals
Interleukin-2 Receptors

Genetic diagnosis for congenital hemolytic anemia

Ohga, S., Jan 1 2016, In : [Rinsho ketsueki] The Japanese journal of clinical hematology. 57, 10, p. 1908-1912 5 p.

Research output: Contribution to journalArticle

Congenital Hemolytic Anemia
Erythrocytes
Anemia
Hemolytic Anemia
Genetic Phenomena

Hemostatic assessment of combined anticoagulant therapy using warfarin and prothrombin complex concentrates in a case of severe protein C deficiency

Ogiwara, K., Nogami, K., Mizumachi, K., Nakagawa, T., Noda, N., Ohga, S. & Shima, M., Jun 20 2019, In : International journal of hematology. 109, 6, p. 650-656 7 p.

Research output: Contribution to journalArticle

Protein C Deficiency
Hemostatics
Warfarin
Anticoagulants
Therapeutics
Ventricular Outflow Obstruction
Ductus Arteriosus
Patient Rights
Parturition
Incidence
1 Citation (Scopus)

High incidence of progressive stenosis in aberrant left subclavian artery with right aortic arch

Muraoka, M., Nagata, H., Hirata, Y., Uike, K., Terashi, E., Morihana, E., Ochiai, M., Fujita, Y., Kato, K., Yamamura, K. & Ohga, S., Mar 1 2018, In : Heart and Vessels. 33, 3, p. 309-315 7 p.

Research output: Contribution to journalArticle

Thoracic Aorta
Pathologic Constriction
Incidence
Vertebral Artery
Parturition