S. Kanzaki

发表

Serum bone alkaline phosphatase isoenzyme levels in normal children and children with growth hormone (GH) deficiency: a potential marker for bone formation and response to GH therapy.

Hiroyuki Tanaka, H. Tobiume, S. Kanzaki, 1997, The Journal of clinical endocrinology and metabolism.

Suppression of nocturnal growth hormone secretion in epilepsy with continuous spike‐waves during slow‐wave sleep

H. Tobiume, S. Kanzaki, K. Iyoda, 1999, Pediatrics international : official journal of the Japan Pediatric Society.

Growth standard charts for Japanese children with mean and standard deviation (SD) values based on the year 2000 national survey

Yoshiya Ito, S. Kanzaki, T. Isojima, 2016, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Effects of N-hexacosanol on nitric oxide synthase system in diabetic rat nephropathy

M. Saito, S. Kanzaki, K. Satoh, 2008, Molecular and Cellular Biochemistry.

OR11-5 A FAMILY WITH SHORT STATURE BORN INTRAUTERINE GROWTH RETARDATION BEARING A NEW MISSENSE MUTATION AT α SUBUNIT OF IGF-I RECEPTOR (R431L)

Yuki Kawashima, S. Kanzaki, T. Kinoshita, 2006 .

Molecular defects in achondroplasia and the effects of growth hormone treatment

S. Kanzaki, T. Moriwake, H. Tanaka, 1999, Acta paediatrica (Oslo, Norway : 1992). Supplement.

Effects of financial support on treatment of adolescents with growth hormone deficiency: a retrospective study in Japan

Hiroyuki Tanaka, K. Takano, Toshiaki Tanaka, 2016, BMC Health Services Research.

Instability of KCNE1‐D85N that Causes Long QT Syndrome: Stabilization by Verapamil

M. Horie, I. Hisatome, K. Higaki, 2014, Pacing and clinical electrophysiology : PACE.

Incidence of pediatric IgA nephropathy

S. Kanzaki, T. Okasora, Y. Utsunomiya, 2003, Pediatric Nephrology.

Successful Treatment of Cyst Infection in an Infant With Autosomal Dominant Polycystic Kidney Disease Using Trimethoprim/Sulfamethoxazole

S. Kanzaki, K. Kitamoto, N. Namba, 2020, Frontiers in Pediatrics.

Urinary glycylprolyl dipeptidyl aminopeptidase (GP‐DAP) in insulin‐dependent diabetic patients

S. Kanzaki, T. Moriwake, Y. Seino, 1992, Acta paediatrica.

Mizoribine oral pulse therapy for a patient with polyarticular juvenile idiopathic arthritis

S. Kanzaki, Y. Utsunomiya, Takuya Hanada, 2006, Pediatrics international : official journal of the Japan Pediatric Society.

Favorable Impact of Growth Hormone Treatment on Cholesterol Levels in Turner Syndrome

K. Tachibana, Hiroyuki Tanaka, K. Fujieda, 2012, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Incidence of diabetes mellitus and neoplasia in Japanese short-statured children treated with growth hormone in the Genetics and Neuroendocrinology of Short Stature International Study (GeNeSIS)

K. Chihara, Hiroyuki Tanaka, K. Ozono, 2017, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Low-vacuum scanning electron microscopy may allow early diagnosis of human renal transplant antibody-mediated rejection.

H. Nakane, S. Kanzaki, K. Kitamoto, 2020, Biomedical research.

Approximate Entropy of Respiratory Movements in Human Newborns during Different Sleep States

E. Shimizu, T. Amisaki, N. Burioka, 2016, Yonago acta medica.

The Japanese Study Group of Insulin Therapy for Childhood and Adolescent Diabetes (JSGIT): initial aims and impact of the family history of type 1 diabetes mellitus in Japanese children

K. Tachibana, Toshikazu Takahashi, I. Yokota, 2001, Pediatric diabetes.

Immunohistochemical characterization of glomerular inflammatory cells and expression of adhesion molecules in anti‐glomerular basement membrane (anti‐GBM) glomerulonephritis induced in WKY rats with monoclonal anti‐GBM antibodies of different subclasses

Tadashi Yamamoto, Y. Sado, S. Kanzaki, 2006, Pathology international.

Growth hormone increases serum 1,25-dihydroxyvitamin D levels and decreases 24,25-dihydroxyvitamin D levels in children with growth hormone deficiency.

S. Wei, S. Kanzaki, T. Ono, 1997, European journal of endocrinology.

Effects of cyclohexenonic long-chain fatty alcohol in type 2 diabetic rat nephropathy.

M. Saito, T. Oite, S. Kanzaki, 2010, Biomedical research.

Variation analysis of β3‐adrenergic receptor and melanocortin‐4 receptor genes in childhood obesity

E. Nanba, Yuki Kawashima, S. Kanzaki, 2007, Pediatrics international : official journal of the Japan Pediatric Society.

EBNA-2-Deleted Epstein-Barr Virus from P3HR-1 Can Infect Rabbits with Lower Efficiency than Prototype Epstein-Barr Virus from B95-8

K. Hayashi, Keiko Nagata, S. Kuwamoto, 2013, Intervirology.

Epstein–Barr virus can infect rabbits by the intranasal or peroral route: An animal model for natural primary EBV infection in humans

K. Hayashi, S. Kuwamoto, Masako Kato, 2010, Journal of medical virology.

Clinical heterogeneity of neonatal intrahepatic cholestasis caused by citrin deficiency: case reports from 16 patients.

T. Saheki, Keiko Kobayashi, S. Kanzaki, 2004, Molecular genetics and metabolism.

High nephritogenicity of monoclonal antibodies belonging to IgG2a and IgG2b subclasses in rat anti-GBM nephritis.

Y. Sado, Y. Ninomiya, S. Kanzaki, 2004, Kidney international.

Gender differences in childhood food preference: Evaluation using a subjective picture choice method

S. Kanzaki, S. Kimura, K. Hanaki, 2014, Pediatrics international : official journal of the Japan Pediatric Society.

Aromatase excess syndrome: identification of cryptic duplications and deletions leading to gain of function of CYP19A1 and assessment of phenotypic determinants.

T. Ogata, G. Binder, S. Kanzaki, 2011, The Journal of clinical endocrinology and metabolism.

Regional rearrangements in chromosome 15q21 cause formation of cryptic promoters for the CYP19 (aromatase) gene.

S. Bulun, R. Schultz, M. Misra, 2007, Human molecular genetics.

Castleman disease in a child with short stature

S. Kanzaki, M. Fujimoto, J. Ueyama, 2012, Pediatrics international : official journal of the Japan Pediatric Society.

Serum propeptide and intact molecular osteocalcin in normal children and children with growth hormone (GH) deficiency: a potential marker of bone growth and response to GH therapy.

Hiroyuki Tanaka, S. Kanzaki, T. Moriwake, 1992, The Journal of clinical endocrinology and metabolism.

1,25-Dihydroxyvitamin D3 stimulates the secretion of insulin-like growth factor binding protein 3 (IGFBP-3) by cultured human osteosarcoma cells.

S. Kanzaki, T. Moriwake, H. Tanaka, 1992, Endocrinology.

Hypothyroidism and hypoparathyroidism in an 11 year old boy with hemochromatosis secondary to aplastic anemia

Y. Takahashi, S. Kanzaki, Y. Seino, 1995, Acta paediatrica Japonica : Overseas edition.

Growth hormone (GH) treatment of GH-deficient children increases serum levels of insulin-like growth factors (IGFs), IGF-binding protein-3 and -5, and bone alkaline phosphatase isoenzyme.

S. Mohan, S. Kanzaki, T. Ono, 1996, Journal of Clinical Endocrinology and Metabolism.

Heterozygous nonsense mutations near the C‐terminal region of IGF1R in two patients with small‐for‐gestational‐age‐related short stature

E. Nanba, S. Kanzaki, M. Fujimoto, 2015, Clinical endocrinology.

Effect of growth hormone on fatty liver in panhypopituitarism

S. Kanzaki, Y. Seino, T. Kubo, 1997, Archives of disease in childhood.

Serum levels of carboxyterminal propeptide of type I procollagen and pyridinoline crosslinked telopeptide of type I collagen in normal children and children with growth hormone (GH) deficiency during GH therapy.

S. Kanzaki, H. Tanaka, Y. Seino, 1995, Bone.

Various phenotypes of short stature with heterozygous IGF-1 receptor (IGF1R) mutations

S. Kanzaki, N. Namba, M. Fujimoto, 2022, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Novel missense mutation in the IGF‐I receptor L2 domain results in intrauterine and postnatal growth retardation

K. Higaki, F. Hakuno, Shin-ichiro Takahashi, 2012, Clinical endocrinology.

Familial short stature with IGF-I receptor gene anomaly.

Shin-ichiro Takahashi, Yuki Kawashima, S. Kanzaki, 2012, Endocrine journal.

Bone Mineral Status in Turner Syndrome

Hiroyuki Tanaka, S. Kanzaki, T. Ono, 1995 .

Cholesterol ester storage disease with a novel LIPA mutation (L264P) that presented massive hepatomegaly: A case report

Y. Eto, K. Murayama, S. Kanzaki, 2016, Hepatology research : the official journal of the Japan Society of Hepatology.

Serum free insulin-like growth factor I (IGF-I), total IGF-I, and IGF-binding protein-3 concentrations in normal children and children with growth hormone deficiency.

S. Kanzaki, Y. Seino, Y. Yamanaka, 1999, The Journal of clinical endocrinology and metabolism.

S. Kanzaki, T. Moriwake, O. Nukada, 1990, Acta paediatrica Japonica : Overseas edition.

Effect of Sex Hormones on Bone Mineral Density in Children

Hiroyuki Tanaka, S. Kanzaki, T. Ono, 1996 .

Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri–Weill dyschondrosteosis

T. Ogata, Hiroyuki Tanaka, Y. Matsubara, 2016, Journal of Human Genetics.

Monday, 27 August 2012

V. V. Ivanenko, E. A. Medvedeva, Michail I. Papafaklis, 2012 .

[Serum levels of intact molecular osteocalcin in children with growth hormone (GH) deficiency during GH therapy: an early predictor of GH therapy].

S. Kanzaki, Y. Seino, T. Kubo, 1994, Nihon Naibunpi Gakkai zasshi.

A novel approach to the histological diagnosis of pediatric nephrotic syndrome by low vacuum scanning electron microscopy.

H. Nakane, S. Kanzaki, T. Kaidoh, 2014, Biomedical research.

Risk factors for mother‐to‐child transmission of hepatitis C virus: Maternal high viral load and fetal exposure in the birth canal

S. Kanzaki, A. Suyama, T. Hoshika, 2012, Hepatology research : the official journal of the Japan Society of Hepatology.

Malignant osteopetrosis treated with high doses of 1α-hydroxyvitamin D3 and interferon gamma

Hiroyuki Tanaka, S. Kanzaki, T. Moriwake, 1993 .

Effect of Sex Hormones on Bone Mineral Density in Children:Is the Increase in Bone Mineral Density during Puberty only due to Rapid Height Gain?

Hiroyuki Tanaka, S. Kanzaki, T. Ono, 1996 .

Morphological diagnosis of Alport syndrome and thin basement membrane nephropathy by low vacuum scanning electron microscopy.

H. Nakane, S. Kanzaki, K. Kitamoto, 2014, Biomedical research.

Mental retardation, spasticity, basal ganglia calcification, cerebral white matter lesions, multiple endocrine defects, telangiectasia and atrophic skin: A new syndrome?

E. Nanba, Y. Maegaki, S. Moriwaki, 2008, Brain and Development.

Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan

K. Tachibana, Hiroyuki Tanaka, K. Ozono, 2015, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Producibility of exfoliative toxin and staphylococcal coagulase types of Staphylococcus aureus strains isolated from skin infections and atopic dermatitis.

S. Kanzaki, H. Akiyama, H. Kanzaki, 1997, Dermatology.

HLA‐class II and class I genotypes among Japanese children with Type 1A diabetes and their families

K. Ihara, T. Ogata, K. Tokunaga, 2012, Pediatric diabetes.

Epidemiological survey of Japanese children infected with hepatitis B and C viruses

S. Kanzaki, K. Shiraki, I. Nagata, 2010, Hepatology research : the official journal of the Japan Society of Hepatology.

Genotype-Structure-Phenotype Correlations of Disease-Associated IGF1R Variants and Similarities to Those of INSR Variants

Y. Okada, T. Tsunoda, T. Kadowaki, 2021, Diabetes.

Effect of growth hormone therapy in children with achondroplasia: growth pattern, hypothalamic-pituitary function, and genotype.

S. Kanzaki, T. Ono, H. Tanaka, 1998, European journal of endocrinology.

Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism.

T. Ogata, A. Umezawa, K. Hata, 2014, Fertility and sterility.

Achondroplasia: Effect of Growth Hormone in 40 Patients

Hiroyuki Tanaka, S. Kanzaki, Y. Seino, 1994 .

Achondroplasia associated with pelvic lipomatosis

Hiroyuki Tanaka, S. Kanzaki, T. Ono, 1999, The Lancet.

1,25-Dihydroxyvitamin D3 stimulates the secretion of insulin-like growth factor binding protein 3 (IGFBP-3) by cultured human osteosarcoma cells.

S. Kanzaki, T. Moriwake, H. Tanaka, 1992, Endocrinology.

Mutation at cleavage site of insulin-like growth factor receptor in a short-stature child born with intrauterine growth retardation.

I. Hisatome, Shin-ichiro Takahashi, E. Nanba, 2005, The Journal of clinical endocrinology and metabolism.

Associated factors in neonatal hypoglycemic brain injury

Y. Kurozawa, Y. Maegaki, S. Kanzaki, 2009, Brain & development (Tokyo. 1979).

An ultrasensitive assay revealed age‐related changes in serum oestradiol at low concentrations in both sexes from infancy to puberty

Hiroyuki Tanaka, Yoshiki Seino, Hiroyuki Tanaka, 2001, Clinical endocrinology.

Increased IRS2 mRNA Expression in SGA Neonates: PCR Analysis of Insulin/IGF Signaling in Cord Blood

E. Nanba, S. Kanzaki, M. Fujimoto, 2017, Journal of the Endocrine Society.

Acute-phase ITIH4 levels distinguish multi-system from single-system Langerhans cell histiocytosis via plasma peptidomics

K. Hayashi, T. Yoshino, J. Gogusev, 2015, Clinical Proteomics.

Growth Hormone (GH) Treatment in Achondroplasia

S. Kanzaki, T. Moriwake, H. Tanaka, 1993, The Journal of pediatric endocrinology.

Clinical Overview of Nephrogenic Diabetes Insipidus Based on a Nationwide Survey in Japan

E. Nanba, Y. Kondo, Yuki Kawashima, 2014, Yonago acta medica.

Variants associated with autoimmune Type 1 diabetes in Japanese children: implications for age‐specific effects of cis‐regulatory haplotypes at 17q12‐q21

K. Ihara, T. Ogata, I. Yokota, 2016, Diabetic medicine : a journal of the British Diabetic Association.

Growth hormone deficiency and empty sella syndrome in a boy with dup(X) (q13.3----q21.2).

S. Kanzaki, T. Moriwake, Y. Seino, 1992, American journal of medical genetics.

Guidelines for care of pregnant women carrying hepatitis C virus and their infants

N. Inaba, S. Kanzaki, T. Morishima, 2008, Pediatrics international : official journal of the Japan Pediatric Society.

The Usefulness of Ultrasensitive Assay for Estradiol in Both Sexes During Childhood

Hiroyuki Tanaka, S. Kanzaki, T. Moriwake, 2000 .

Analysis of serum thyrotropin dynamics after TRH stimulation in normal children

S. Kanzaki, H. Kimoto, K. Araki, 1984 .

Partial trisomies 9 and 4 resulting from maternal translocation t(4; 9) (q25?; q13)

Y. Kodama, S. Kanzaki, K. Narahara, 1981, The Japanese Journal of Human Genetics.

Effect of lactational exposure to 1,2,3,4‐ tetrachlorodibenzo‐p‐dioxin on cytochrome P‐450 1A1 mRNA in the neonatal rat liver: Quantitative analysis by the competitive RT‐PCR method

S. Kanzaki, Y. Tazawa, E. Ueta, 2001, Pediatrics international : official journal of the Japan Pediatric Society.

Effect of Growth Hormone Treatment on Quality of Life in Japanese Children with Growth Hormone Deficiency: An Analysis from a Prospective Observational Study

K. Chihara, Hiroyuki Tanaka, K. Ozono, 2014, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

An observational study of the effectiveness and safety of growth hormone (Humatrope(®)) treatment in Japanese children with growth hormone deficiency or Turner syndrome.

K. Chihara, Hiroyuki Tanaka, K. Fujieda, 2013, Endocrine journal.

Thyroid-stimulating antibody in a patient with euthyroid Graves' disease.

S. Kanzaki, T. Moriwake, Y. Seino, 2000, Endocrine journal.

Epstein–Barr virus-associated posttransplant lymphoproliferative disorder involving the central nervous system following autologous hematopoietic stem cell transplantation for neuroblastoma

K. Hayashi, S. Kanzaki, M. Fujimoto, 2014, SpringerPlus.

Late-onset adrenal hypoplasia congenita caused by a novel mutation of the DAX-1 gene

Yuki Kawashima, S. Kanzaki, T. Kinoshita, 2009, European Journal of Pediatrics.

Characterization of the ileal muscarinic receptor system in 70-week-old type II Goto-Kakizaki diabetic rats; effects of cyclohexenonic long-chain fatty alcohol.

M. Saito, S. Kanzaki, K. Satoh, 2009, European journal of pharmacology.

Pericentric inversion inv(2) (p11.2q21) associated with Treacher Collins−Franceschetti syndrome

Yuki Kawashima, S. Kanzaki, I. Nagata, 2002, Pediatrics international : official journal of the Japan Pediatric Society.

Secretion of osteocalcin and its propeptide from human osteoblastic cells: Dissociation of the secretory patterns of osteocalcin and its propeptide

S. Kanzaki, Y. Seino, K. Hosoda, 1993, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Fluctuating liver functions in siblings with MPV17 mutations and possible improvement associated with dietary and pharmaceutical treatments targeting respiratory chain complex II.

Y. Okazaki, A. Ohtake, K. Murayama, 2009, Molecular genetics and metabolism.

Early predictors of status epilepticus-associated mortality and morbidity in children

Y. Kurozawa, Y. Maegaki, M. Urushibara, 2015, Brain and Development.

Leprechaunism (Donohue syndrome): a case bearing novel compound heterozygous mutations in the insulin receptor gene.

Yuki Kawashima, S. Kanzaki, M. Fujimoto, 2013, Endocrine journal.

Production of thyrotropin receptor antibodies in acute phase of infectious mononucleosis due to Epstein–Barr virus primary infection: a case report of a child

K. Hayashi, Keiko Nagata, Keisuke Kumata, 2015, SpringerPlus.

Response of anti‐oxidant enzymes mRNA in the neonatal rat liver exposed to 1,2,3,4‐tetrachlorodibenzo‐p‐dioxin via lactation

E. Nanba, S. Kanzaki, Y. Kono, 2002, Pediatrics international : official journal of the Japan Pediatric Society.

Familial short stature is associated with a novel dominant‐negative heterozygous insulin‐like growth factor 1 receptor (IGF1R) mutation

F. Hakuno, Shin-ichiro Takahashi, T. Fukushima, 2014, Clinical endocrinology.