T. Futatani

发表

Clinical and genetic analyses of presumed shwachman-diamond syndrome in Japan

H. Kanegane, H. Yoneyama, J. Kamizono, 2006, International journal of hematology.

Screening of the Bruton Tyrosine Kinase (BTK) Gene Mutations in 13 Iranian Patients with Presumed X-Linked Agammaglobulinemia.

T. Miyawaki, N. Rezaei, A. Aghamohammadi, 2004, Iranian journal of allergy, asthma, and immunology.

A novel immunoregulatory protein in human colostrum, syntenin-1, for promoting the development of IgA-producing cells from cord blood B cells.

H. Kanegane, Taketoshi Yoshida, T. Miyawaki, 2009, International immunology.

Deficient expression of Bruton's tyrosine kinase in monocytes from X-linked agammaglobulinemia as evaluated by a flow cytometric analysis and its clinical application to carrier detection.

M. Kurimoto, T. Kunikata, H. Matsuoka, 1998, Blood.

Clinical and mutational characteristics of X-linked agammaglobulinemia and its carrier identified by flow cytometric assessment combined with genetic analysis.

H. Kanegane, T. Miyawaki, T. Kubota, 2001, The Journal of allergy and clinical immunology.

Bruton's tyrosine kinase is present in normal platelets and its absence identifies patients with X‐linked agammaglobulinaemia and carrier females

H. Ochs, Y. Baba, S. Tsukada, 2001 .

SCN5A variants in Japanese patients with left ventricular noncompaction and arrhythmia.

J. Towbin, Kazuhiro Watanabe, N. Bowles, 2008, Molecular genetics and metabolism.

Three-Dimensional Computed Tomographic Findings of Bilateral Tracheal Bronchus

F. Ichida, O. Higuchi, T. Futatani, 2008, Pediatric Cardiology.

Neutrophils and Mononuclear Cells Express Vascular Endothelial Growth Factor in Acute Kawasaki Disease: Its Possible Role in Progression of Coronary Artery Lesions

H. Kanegane, I. Hashimoto, Taketoshi Yoshida, 2001, Pediatric Research.

Capillary Blood Ketone Levels as an Indicator of Inadequate Breast Milk Intake in the Early Neonatal Period

T. Futatani, N. Igarashi, S. Fujita, 2017, The Journal of pediatrics.

Long QT syndrome with a de novo CALM2 mutation in a 4‐year‐old boy

M. Horie, S. Ohno, T. Futatani, 2019, Pediatrics international : official journal of the Japan Pediatric Society.

Autoimmune lymphoproliferative syndrome presenting with glomerulonephritis

H. Kanegane, T. Miyawaki, H. Matsukura, 2003, Pediatric Nephrology.

Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy’s disease

H. Kanegane, T. Miyawaki, F. Ichida, 2008, Pediatrics international : official journal of the Japan Pediatric Society.

Novel Igalpha (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia.

H. Kanegane, O. Sanal, I. Tezcan, 2002, American journal of medical genetics.

Developmental changes of FOXP3-expressing CD4+CD25+ regulatory T cells and their impairment in patients with FOXP3 gene mutations.

H. Kanegane, H. Ochs, A. Banham, 2007, Clinical immunology.

Expression of myeloid-related protein-8 and -14 in patients with acute Kawasaki disease.

D. Foell, I. Hashimoto, Kazuhiro Watanabe, 2006, Journal of the American College of Cardiology.

Commotio Cordis Presenting as a Temporary Complete Atrioventricular Block in a 2-Year-Old Girl With Congenitally Corrected Transposition of the great Arteries

T. Futatani, A. Toga, N. Igarashi, 2011, Pediatric Cardiology.

Primary Immunodeficiency Diseases Report of an IUIS Scientific Committee

H. Kanegane, T. Miyawaki, T. Futatani, 1999 .

[Agammaglobulinemia as early B cell defects].

H. Kanegane, T. Miyawaki, T. Futatani, 2000, Nihon Rinsho Men'eki Gakkai kaishi = Japanese journal of clinical immunology.

Exclusive breast‐feeding and postnatal changes in blood sodium, ketone, and glucose levels

T. Futatani, N. Igarashi, S. Fujita, 2019, Pediatrics international : official journal of the Japan Pediatric Society.

Point mutation in intron 11 of Bruton’s tyrosine kinase in atypical X‐linked agammaglobulinemia

H. Kanegane, T. Miyawaki, T. Futatani, 2000, Pediatrics international : official journal of the Japan Pediatric Society.

Toll-like receptor signaling is impaired in dendritic cells from patients with X-linked agammaglobulinemia.

H. Kanegane, T. Kaisho, T. Miyawaki, 2008, Clinical immunology.

Virus myocarditis in a 1‐month‐old boy presenting as two types of paroxysmal supraventricular tachycardia

T. Futatani, N. Igarashi, S. Fujita, 2017, Pediatrics international : official journal of the Japan Pediatric Society.

Fetal closed head injuries following maternal motor vehicle accident

Y. Hata, N. Nishida, T. Futatani, 2018, Medicine.

Identification of mutations in the Bruton's tyrosine kinase gene, including a novel genomic rearrangements resulting in large deletion, in Korean X-linked agammaglobulinemia patients

H. Kanegane, T. Miyawaki, K. Ahn, 2003, Journal of Human Genetics.

Severe Neutropenia in Japanese Patients with X-Linked Agammaglobulinemia

H. Kanegane, T. Miyawaki, Hiromichi Taneichi, 2005, Journal of Clinical Immunology.

Impact of prematurity and the CTG repeat length on outcomes in congenital myotonic dystrophy

Kenta Matsumura, Taketoshi Yoshida, M. Kageyama, 2020, BMC Research Notes.

X‐linked lymphoproliferative syndrome presenting with systemic lymphocytic vasculitis

H. Kanegane, K. Ohshima, T. Miyawaki, 2005, American journal of hematology.

Predominance of Th2‐promoting dendritic cells in early human pregnancy decidua

Y. Sasaki, M. Sakai, S. Saito, 2003, Journal of leukocyte biology.

Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry

H. Kanegane, T. Miyawaki, A. Komiyama, 2000, Clinical and experimental immunology.

H. Ochs, E. Stiehm, D. Rawlings, 2001, The Journal of pediatrics.

Absence of memory B cells in patients with common variable immunodeficiency.

H. Ochs, T. Miyawaki, S. Koyasu, 2002, Clinical immunology.

A case of body stalk anomaly arising in the second baby of a triplet pregnancy after in-vitro fertilization and embryo transfer

Y. Sasaki, M. Sakai, S. Saito, 2003, Pediatric Surgery International.

Mutational analysis of theWASP gene in 2 Korean families with Wiskott-Aldrich syndrome

H. Kanegane, T. Miyawaki, S. Nonoyama, 2003, International journal of hematology.

Survival of wild polio by a patient with XLA.

H. Ochs, J. Winkelstein, T. Futatani, 2002, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Role of transforming growth factor-beta in breast milk for initiation of IgA production in newborn infants.

H. Kanegane, Taketoshi Yoshida, T. Miyawaki, 2004, Early human development.

Two infants with mild, atypical clinical features of Kagami-Ogata syndrome caused by epimutation.

R. Kosaki, T. Futatani, M. Kagami, 2022, European journal of medical genetics.

Ganciclovir Therapy for Congenital Cytomegalovirus Infection in Six Infants

H. Kanegane, M. Hayakawa, T. Morishima, 2005, The Pediatric infectious disease journal.

Platelet‐derived growth factor may be associated with fibrosis in a Down syndrome patient with transient myeloproliferative disorder

K. Tsuneyama, H. Kanegane, R. Kanezaki, 2008, European journal of haematology.

A case of congenital midline cervical cleft with congenital heart disease.

K. Tsukada, T. Futatani, I. Hashimoto, 2003, Journal of pediatric surgery.

X-linked thrombocytopenia identified by flow cytometric demonstration of defective Wiskott-Aldrich syndrome protein in lymphocytes.

H. Kanegane, H. Ochs, T. Miyawaki, 2000, Blood.

[Intravenous immunoglobulin replacement therapy in X-linked agammaglobulinemia].

H. Kanegane, T. Miyawaki, T. Futatani, 2002, Nihon Rinsho Men'eki Gakkai kaishi = Japanese journal of clinical immunology.

Hyperinsulinemic hypoglycemia in Beckwith–Wiedemann, Sotos, and Kabuki syndromes: A nationwide survey in Japan

K. Ihara, T. Hara, H. Mizumoto, 2017, American journal of medical genetics. Part A.

Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes

H. Kanegane, H. Ochs, M. Yamada, 2011, Journal of Human Genetics.

Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity.

Toshio Miyawaki, Rui Chen, Noriyuki Haneda, 2005, Molecular genetics and metabolism.

Bruton's Tyrosine Kinase (BTK) Is Present in Normal Platelets, and Its Absence Identifies Patients with X-Linked Agammaglobulinemia (XLA) and Carrier Females

H. Ochs, Y. Baba, A. Oda, 1999, British journal of haematology.

Catecholaminergic polymorphic ventricular tachycardia managed as orthostatic dysregulation and epilepsy in 11‐ and 15‐year‐old sisters

M. Horie, S. Ohno, T. Futatani, 2018, Pediatrics international : official journal of the Japan Pediatric Society.

Left atrium thrombus in an extremely low‐birthweight infant with late‐onset circulatory dysfunction

T. Futatani, N. Igarashi, S. Fujita, 2012, Pediatrics international : official journal of the Japan Pediatric Society.

Contiguous X-chromosome Deletion Syndrome Encompassing the BTK, TIMM8A, TAF7L, and DRP2 Genes

H. Ochs, K. Sullivan, A. Šedivá, 2007, Journal of Clinical Immunology.

Congenital corneal staphyloma associated with aphakia.

Y. Nagaki, S. Yanagisawa, S. Hayasaka, 2004, Journal of pediatric ophthalmology and strabismus.

Atypical X-linked agammaglobulinemia diagnosed in three adults.

H. Kanegane, T. Yamadori, T. Miyawaki, 1999, Internal medicine.

Novel mutations in a Japanese patient with CD19 deficiency

H. Kanegane, T. Miyawaki, K. Agematsu, 2007, Genes and Immunity.

The efficacy of pacemaker implantation for extracardiac total cavopulmonary connection in a pediatric patient with bradycardia-tachycardia syndrome.

A. Murata, T. Futatani, N. Igarashi, 2021, Journal of cardiology cases.

Effect of postnatal hydrocortisone on 18-month neurodevelopmental outcomes in very-low-birth-weight infants.

S. Saito, Taketoshi Yoshida, Yosuke Ono, 2018, Pediatrics and neonatology.

Identification of mutations of Bruton's tyrosine kinase gene (BTK) in Brazilian patients with X‐linked agammaglobulinemia

H. Kanegane, T. Miyawaki, J. Pinto, 2002, Human mutation.

Role of transforming growth factor-beta in breast milk for initiation of IgA production in newborn infants.

H. Kanegane, Taketoshi Yoshida, T. Miyawaki, 2004, Early human development.