Takehisa Yamamoto

发表

Structure equation model and neural network analyses to predict coronary artery lesions in Kawasaki disease: a single-centre retrospective study

J. Azuma, Takehisa Yamamoto, Motoaki Nitta, 2020, Scientific Reports.

Fibroblast growth factor 23 in oncogenic osteomalacia and X-linked hypophosphatemia.

K. White, M. Econs, H. Jüppner, 2003, The New England journal of medicine.

Treatment with recombinant IL-2 for recurrent respiratory infection in a case of cartilage-hair hypoplasia with autoimmune hemolytic anemia

T. Okamura, K. Ozono, S. Okada, 2000, Journal of Bone and Mineral Metabolism.

Serum immunoglobulin G subclass levels and estimated clinical severity caused by possible influenza A (H1N1) pdm 2009 infection

T. Kase, H. Kawashima, Takehisa Yamamoto, 2013, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.

Complete oculocerebrorenal phenotype of Lowe syndrome in a female patient with half reduction of inositol polyphosphate 5-phosphatase

Takehisa Yamamoto, Y. Hasegawa, T. Shimotsuji, 2019, CEN Case Reports.

Prognostic factors for acute encephalopathy with bright tree appearance

K. Kagitani-Shimono, J. Azuma, K. Ozono, 2015, Brain and Development.

Prediction of non-responsiveness to standard high-dose gamma-globulin therapy in patients with acute Kawasaki disease before starting initial treatment

S. Kurotobi, T. Sano, S. Kogaki, 2006, European Journal of Pediatrics.

Pulse methylprednisolone with gammaglobulin as an initial treatment for acute Kawasaki disease

T. Sano, T. Nishigaki, K. Okada, 2009, European Journal of Pediatrics.

Two girls with a neonatal screening-negative 21-hydroxylase deficiency requiring treatment with hydrocortisone for virilization in late childhood

K. Ozono, T. Hasegawa, Shinsuke Onuma, 2021, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Decrease in serum FGF23 levels after intravenous infusion of pamidronate in patients with osteogenesis imperfecta

K. Ozono, T. Kubota, N. Namba, 2011, Journal of Bone and Mineral Metabolism.

Serum Fibroblast Growth Factor 23 Is a Useful Marker to Distinguish Vitamin D-Deficient Rickets from Hypophosphatemic Rickets

K. Ozono, T. Kubota, N. Namba, 2014, Hormone Research in Paediatrics.

Increased Serum IL-10 and Endothelin Levels in Hemolytic Uremic Syndrome Caused by Escherichia coli O157

T. Honda, S. Okada, Takehisa Yamamoto, 2000, Nephron.

Severe arterial hypertension: a possible complication of McCune-Albright syndrome

S. Ida, K. Ozono, Y. Imanishi, 2009, European Journal of Pediatrics.

The Role of Cytokines for the Pathogenesis of Hemolytic Uremic Syndrome Caused by Escherichia coli O 157:H7 Infections.

M. Monden, T. Shimazu, T. Honda, 1998 .

Risk factors for neurological complications in complete hemolytic uremic syndrome caused by Escherichia coli O157

K. Ozono, S. Okada, Takehisa Yamamoto, 2009, Pediatrics international : official journal of the Japan Pediatric Society.

Serum calcitriol levels in a patient with X-linked hypophosphatemia complicated by autosomal dominant polycystic kidney disease

K. Ozono, T. Kubota, T. Michigami, 2017, CEN Case Reports.

Molecular Bases of Diseases Characterized by Hypophosphatemia and Phosphaturia: New Understanding

K. Ozono, T. Michigami, N. Namba, 2006, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

The role of IGF-I in phosphate therapy for the short stature of patients with hypophosphatemic vitamin D-resistant rickets

K. Ozono, T. Michigami, S. Okada, 2005, Journal of Bone and Mineral Metabolism.

The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune–Albright syndrome

H. Jüppner, M. Inaba, K. Ozono, 2004, Journal of Bone and Mineral Metabolism.

Hypophosphatemic rickets accompanying McCune–Albright syndrome: evidence that a humoral factor causes hypophosphatemia

H. Yoshikawa, K. Ozono, E. Takeda, 2001, Journal of Bone and Mineral Metabolism.

Alkaline phosphatase in pediatric patients with genu varum caused by vitamin D-deficient rickets.

K. Ozono, T. Kubota, T. Michigami, 2021, Endocrine journal.

Early therapy with neuraminidase inhibitors for influenza A (H1N1) pdm 2009 infection

T. Kase, N. Okabe, Takehisa Yamamoto, 2013, Pediatrics international : official journal of the Japan Pediatric Society.

Hereditary hypophosphatemic rickets with hypercalciuria: a study for the phosphate transporter gene type IIc and osteoblastic function

K. Ozono, K. Miyamoto, T. Michigami, 2007, Journal of Bone and Mineral Metabolism.

Clinical approach to clarifying the mechanism of abnormal bone metabolism in McCune–Albright syndrome

Takehisa Yamamoto, 2005, Journal of Bone and Mineral Metabolism.

Urinary β2-microglobulin as an early marker of infantile enterovirus and human parechovirus infections

J. Azuma, K. Ozono, Takehisa Yamamoto, 2018, Medicine.

A Case of Vitamin D Dependency Type I

K. Ozono, Y. Seino, S. Nakajima, 1992 .

Fat distribution in short‐stature children born small for gestational age

Y. Etani, S. Ida, M. Kawai, 2020, Pediatrics international : official journal of the Japan Pediatric Society.

Treatment of renal osteodystrophy in children with 1αOHD3 and 24, 25(OH)2D3

Hiroyuki Tanaka, Y. Seino, M. Ishida, 1988, Journal of Bone and Mineral Metabolism.

Alendronate and pharmacological doses of 1α OHD3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia

H. Yoshikawa, K. Ozono, S. Okada, 2002, Journal of Bone and Mineral Metabolism.

Hypophosphatemic osteomalacia and bone sclerosis caused by a novel homozygous mutation of the FAM20C gene in an elderly man with a mild variant of Raine syndrome.

F. Glorieux, K. Ozono, Y. Imanishi, 2014, Bone.

Advanced Glycation Endproducts Stimulate Interleukin‐6 Production by Human Bone‐Derived Cells

T. Kishimoto, H. Yamamoto, S. Kasayama, 1997, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

In vivo osteogenic activity of isolated human bone cells

F. Glorieux, Takehisa Yamamoto, B. Ecarot, 1991, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Cost-effectiveness of Hepatitis B Serology Testing Before Hepatitis B Vaccination in the Akha Tribal Children in Northeastern Thailand

Saeko Morikawa, T. Kase, Takehisa Yamamoto, 2011 .

Early juvenile Tay–Sachs disease with atypical symptoms

J. Azuma, N. Sakai, Takehisa Yamamoto, 2019, Pediatrics International.

Hypophosphatemic Rickets Accompanying Congenital Microvillous Atrophy

Takehisa Yamamoto, M. Shima, H. Tajiri, 1998, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Development of scoliosis in young children with osteogenesis imperfecta undergoing intravenous bisphosphonate therapy

H. Yoshikawa, T. Kaito, T. Makino, 2018, Journal of bone and mineral metabolism.

Alice in Wonderland syndrome caused by the 2009 pandemic H1N1 influenza A virus.

Saeko Morikawa, T. Kase, Takehisa Yamamoto, 2011, The Pediatric infectious disease journal.

Two cases of hyponatremic-hypertensive syndrome in childhood with renovascular hypertension

M. Hattori, H. Tamai, H. Katayama, 2006, European Journal of Pediatrics.

Elevated Bone Turnover in an Infantile Patient with Mucolipidosis II; No Association with Hyperparathyroidism

K. Ozono, T. Otomo, Takehisa Yamamoto, 2011, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

[Updates on rickets and osteomalacia: the therapy for FGF23 related rickets].

Takehisa Yamamoto, 2013, Clinical calcium.

Increased Interleukin‐6 Production in Mouse Osteoblastic MC3T3‐E1 Cells Expressing Activating Mutant of the Stimulatory G Protein

T. Kishimoto, S. Kurebayashi, S. Kasayama, 1998, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

IgG3 deficiency and severity of 2009 pandemic H1N1 influenza

T. Kase, Takehisa Yamamoto, T. Shimotsuji, 2012, Pediatrics international : official journal of the Japan Pediatric Society.

Diagnosis of X‐linked hypophosphatemia vitamin D resistant rickets

T. Yamamoto, Takehisa Yamamoto, 1997, Acta paediatrica Japonica : Overseas edition.

A Case of Primary Hyperparathyroidism in Childhood Found by a Chance Hematuria

K. Ozono, Takehisa Yamamoto, T. Shimotsuji, 2007, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Overlapping Myocarditis and Postural Orthostatic Tachycardia Syndrome After COVID-19 Messenger RNA Vaccination: A Case Report

J. Azuma, Takehisa Yamamoto, Y. Hasegawa, 2022, Cureus.

A distinct subtype of “metatropic dysplasia variant” characterised by advanced carpal skeletal age and subluxation of the radial heads

K. Ozono, G. Nishimura, N. Aida, 1998, Pediatric Radiology.

FGF-23 is a circulating factor that is elevated in oncogenic osteomalacia and X-linked hypophosphatemic rickets.

K. White, M. Econs, J. Lavigne, 2002 .

Bone marrow-derived osteoclast-like cells from a patient with craniometaphyseal dysplasia lack expression of osteoclast-reactive vacuolar proton pump.

M. Okada, N. Kurihara, K. Ozono, 1993, The Journal of clinical investigation.

24R,25-dihydroxyvitamin D3 increases cyclic GMP contents, leading to an enhancement of osteocalcin synthesis by 1,25-dihydroxyvitamin D3 in cultured human osteoblastic cells.

K. Ozono, Takehisa Yamamoto, K. Yamaoka, 1998, Experimental cell research.

Marked hypercalcemia in a patient with hypocalciuric hypercalcemia without a mutation in the calcium-sensing receptor gene.

M. Menju, T. Maruyama, I. Konishi, 2002, Internal medicine.