Lista de obras - Tsuyoshi Isojima - Dominio Público Uruguay

A familial case of nail patella syndrome with a heterozygous in-frame indel mutation in the LIM domain of LMX1B.

artículo científico publicado en 2017

A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2.

artículo científico publicado en 2014

Alterations in physique among young children after the Great East Japan Earthquake: Results from a nationwide survey.

artículo científico publicado en 2017

Association of vitamin D-related gene polymorphisms with manifestation of vitamin D deficiency in children

artículo científico publicado en 2012

Design of the Nationwide Nursery School Survey on Child Health Throughout the Great East Japan Earthquake.

artículo científico publicado en 2015

Design of the health examination survey on early childhood physical growth in the Great East Japan Earthquake affected areas

artículo científico publicado en 2017

Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array

artículo científico publicado en 2015

Development of disease-specific growth charts in Turner syndrome and Noonan syndrome

artículo científico publicado en 2017

Development of waist circumference percentiles for Japanese children and an examination of their screening utility for childhood metabolic syndrome: a population-based cross-sectional study

artículo científico publicado en 2015

Disease prevalence among nursery school children after the Great East Japan earthquake.

artículo científico publicado en 2017

Disease-specific Growth Charts of Marfan Syndrome Patients in Korea

artículo científico publicado en 2015

Disease-specific growth charts for Korean infants with Prader-Willi syndrome

artículo científico publicado en 2014

Earlier BMI rebound and lower pre-rebound BMI as risk of obesity among Japanese preschool children.

artículo científico publicado en 2017

Early excessive growth with distinct seasonality in preschool obesity

artículo científico publicado en 2018

Effect of the Fukushima earthquake on weight in early childhood: a retrospective analysis

artículo científico publicado en 2018

Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia.

artículo científico publicado en 2017

Growth hormone deficiency: a possible complication of glucose transporter 1 deficiency?

artículo científico publicado en 2012

Growth references for Japanese individuals with Noonan syndrome.

artículo científico publicado en 2015

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

artículo científico publicado en 2016

Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR) caused by a VDR mutation: A novel mechanism of dominant inheritance

artículo científico publicado en 2015

Impact of the Great East Japan Earthquake on Body Mass Index, Weight, and Height of Infants and Toddlers: An Infant Survey.

artículo científico publicado en 2018

Impact of the great east Japan earthquake on the body mass index of preschool children: a nationwide nursery school survey

artículo científico publicado en 2016

Inconsistent determination of overweight by two anthropometric indices in girls with Turner syndrome

scientific article published on 17 November 2008

Kenny-Caffey syndrome and its related syndromes

artículo científico publicado en 2015

LMX1B mutation with residual transcriptional activity as a cause of isolated glomerulopathy

artículo científico publicado en 2013

Longitudinal changes in body mass index of children affected by the Great East Japan Earthquake.

artículo científico publicado en 2017

Maternal Undernutrition and Breast Milk Macronutrient Content Are Not Associated with Weight in Breastfed Infants at 1 and 3 Months after Delivery

artículo científico publicado en 2019

Mineral status of premature infants in early life and linear growth at age 3

scientific article published on 10 September 2015

New reference growth charts for Japanese girls with Turner syndrome

artículo científico publicado en 2009

Nonclassic steroid 21-hydroxylase deficiency due to a homozygous V281L mutation in CYP21A2 detected by the neonatal mass-screening program in Japan

artículo científico publicado en 2007

Nonosmotic secretion of arginine vasopressin and salt loss in hyponatremia in Kawasaki disease

artículo científico publicado en 2020

Novel DHCR7 mutation in a case of Smith-Lemli-Opitz syndrome showing 46,XY disorder of sex development.

artículo científico publicado en 2017

Painful thyroiditis and subsequent atrophic hypothyroidism after cord blood transfusion

artículo científico publicado en 2011

Partial monosomy of 10p and duplication of another chromosome in two patients

Prolonged elevated body mass index in preschool children after the Great East Japan Earthquake.

artículo científico publicado en 2017

Proposal of new auxological standards for Japanese girls with turner syndrome.

artículo científico publicado en 2010

Revision of the Growth References for Japanese Girls with Turner Syndrome

scientific article published on 01 March 2017

Spectrum of LMX1B mutations: from nail-patella syndrome to isolated nephropathy.

artículo científico publicado en 2016

Standardized centile curves and reference intervals of serum insulin-like growth factor-I (IGF-I) levels in a normal Japanese population using the LMS method

artículo científico publicado en 2012

Steroid-resistant nephrotic syndrome as the initial presentation of nail-patella syndrome: a case of a de novo LMX1B mutation.

artículo científico publicado en 2017

Successful intermittent intravenous calcium treatment via the peripheral route in a patient with hereditary vitamin D-resistant rickets and alopecia

artículo científico publicado en 2015

Systemic lupus erythematosus complicated with liver cirrhosis in a patient with Papillon-Lefèvre syndrome

artículo científico publicado en 2014

Systemic lupus erythematosus presenting with mixed-type fulminant autoimmune hemolytic anemia

scholarly article by Yoko Hirano et al published 19 February 2016 in Pediatrics International

The response to growth hormone treatment in prepubertal children with growth hormone deficiency in Japan: Comparing three consecutive years of treatment data of The Foundation for Growth Science in Japan between the 1990s and 2000s.

artículo científico publicado en 2017

The value of anthropometric indices for childhood obesity in Japan

artículo científico publicado en 2019

Trace element levels in mature breast milk of recent lactating Japanese women

artículo científico publicado en 2020

Trends in age and anthropometric data at start of growth hormone treatment for girls with Turner syndrome in Japan

artículo científico publicado en 2008

Vitamin D-Deficient Rickets in Japan

artículo científico publicado en 2017

Lista de obras de Tsuyoshi Isojima

A familial case of nail patella syndrome with a heterozygous in-frame indel mutation in the LIM domain of LMX1B.

A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2.

Alterations in physique among young children after the Great East Japan Earthquake: Results from a nationwide survey.

Association of vitamin D-related gene polymorphisms with manifestation of vitamin D deficiency in children

Design of the Nationwide Nursery School Survey on Child Health Throughout the Great East Japan Earthquake.

Design of the health examination survey on early childhood physical growth in the Great East Japan Earthquake affected areas

Detection of Hereditary 1,25-Hydroxyvitamin D-Resistant Rickets Caused by Uniparental Disomy of Chromosome 12 Using Genome-Wide Single Nucleotide Polymorphism Array

Development of disease-specific growth charts in Turner syndrome and Noonan syndrome

Development of waist circumference percentiles for Japanese children and an examination of their screening utility for childhood metabolic syndrome: a population-based cross-sectional study

Disease prevalence among nursery school children after the Great East Japan earthquake.

Disease-specific Growth Charts of Marfan Syndrome Patients in Korea

Disease-specific growth charts for Korean infants with Prader-Willi syndrome

Earlier BMI rebound and lower pre-rebound BMI as risk of obesity among Japanese preschool children.

Early excessive growth with distinct seasonality in preschool obesity

Effect of the Fukushima earthquake on weight in early childhood: a retrospective analysis

Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia.

Growth hormone deficiency: a possible complication of glucose transporter 1 deficiency?

Growth references for Japanese individuals with Noonan syndrome.

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

Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR) caused by a VDR mutation: A novel mechanism of dominant inheritance

Impact of the Great East Japan Earthquake on Body Mass Index, Weight, and Height of Infants and Toddlers: An Infant Survey.

Impact of the great east Japan earthquake on the body mass index of preschool children: a nationwide nursery school survey

Inconsistent determination of overweight by two anthropometric indices in girls with Turner syndrome

Kenny-Caffey syndrome and its related syndromes

LMX1B mutation with residual transcriptional activity as a cause of isolated glomerulopathy

Longitudinal changes in body mass index of children affected by the Great East Japan Earthquake.

Maternal Undernutrition and Breast Milk Macronutrient Content Are Not Associated with Weight in Breastfed Infants at 1 and 3 Months after Delivery

Mineral status of premature infants in early life and linear growth at age 3

New reference growth charts for Japanese girls with Turner syndrome

Nonclassic steroid 21-hydroxylase deficiency due to a homozygous V281L mutation in CYP21A2 detected by the neonatal mass-screening program in Japan

Nonosmotic secretion of arginine vasopressin and salt loss in hyponatremia in Kawasaki disease

Novel DHCR7 mutation in a case of Smith-Lemli-Opitz syndrome showing 46,XY disorder of sex development.

Painful thyroiditis and subsequent atrophic hypothyroidism after cord blood transfusion

Partial monosomy of 10p and duplication of another chromosome in two patients

Prolonged elevated body mass index in preschool children after the Great East Japan Earthquake.

Proposal of new auxological standards for Japanese girls with turner syndrome.

Revision of the Growth References for Japanese Girls with Turner Syndrome

Spectrum of LMX1B mutations: from nail-patella syndrome to isolated nephropathy.

Standardized centile curves and reference intervals of serum insulin-like growth factor-I (IGF-I) levels in a normal Japanese population using the LMS method

Steroid-resistant nephrotic syndrome as the initial presentation of nail-patella syndrome: a case of a de novo LMX1B mutation.

Successful intermittent intravenous calcium treatment via the peripheral route in a patient with hereditary vitamin D-resistant rickets and alopecia

Systemic lupus erythematosus complicated with liver cirrhosis in a patient with Papillon-Lefèvre syndrome

Systemic lupus erythematosus presenting with mixed-type fulminant autoimmune hemolytic anemia

The response to growth hormone treatment in prepubertal children with growth hormone deficiency in Japan: Comparing three consecutive years of treatment data of The Foundation for Growth Science in Japan between the 1990s and 2000s.

The value of anthropometric indices for childhood obesity in Japan

Trace element levels in mature breast milk of recent lactating Japanese women

Trends in age and anthropometric data at start of growth hormone treatment for girls with Turner syndrome in Japan

Vitamin D-Deficient Rickets in Japan