Cargando…

Serum IGF-1 and IGFBP-3 Levels in Healthy Children Between 0 and 6 Years of Age

Objective: Along with growth hormone (GH) levels, measurements of serum insulin-like growth factor-1 (IGF-1) and IGF-binding protein-3 (IGFBP-3) are used in the diagnosis of GH deficiency and in monitoring the efficacy and safety of long-term GH treatment. The purpose of the present study was to est...

Descripción completa

Detalles Bibliográficos
Autores principales:	Yüksel, Bilgin, Özbek, M. Nuri, Mungan, Neslihan Önenli, Darendeliler, Feyza, Budan, Bahar, Bideci, Aysun, Çetinkaya, Ergün, Berberoğlu, Merih, Evliyaoğlu, Olcay, Yeşilkaya, Ediz, Arslanoğlu, İlknur, Darcan, Şükran, Bundak, Ruveyda, Ercan, Olcay
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Galenos Publishing 2011
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3119446/ https://www.ncbi.nlm.nih.gov/pubmed/21750637 http://dx.doi.org/10.4274/jcrpe.v3i2.17

Ejemplares similares

Evaluation of Permanent Growth Hormone Deficiency (GHD) in Young Adults with Childhood Onset GHD: A multicenter study
por: Berberoğlu, Merih, et al.
Publicado: (2008)

Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia
por: Savaş-Erdeve, Şenay, et al.
Publicado: (2021)

Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey
por: Poyrazoğlu, Şükran, et al.
Publicado: (2015)

Puberty and Pubertal Growth in Healthy Turkish Girls: No evidence for secular trend
por: Bundak, Rüveyde, et al.
Publicado: (2008)

Evaluation of Thyroid Functions with Respect to Iodine Status and TRH Test in Chronic Autoimmune Thyroiditis
por: Ergür, Ayça Törel, et al.
Publicado: (2011)

Long−Term Follow−Up of a Pseudohypoparathyroidism Type 1A Patient with Missense Mutation (Pro115Ser) in Exon 5
por: Erdeve, Şenay Savaş, et al.
Publicado: (2010)

Z-Score Reference Values for Height in Turkish Children Aged 6 to 18 Years
por: Günöz, Hülya, et al.
Publicado: (2014)

Epidemiologic Features of Type 1 Diabetic Patients between 0 and 18 Years of Age in İstanbul City
por: Demir, Fikri, et al.
Publicado: (2015)

Reference Values for Weight, Height, Head Circumference, and Body Mass Index in Turkish Children
por: Neyzi, Olcay, et al.
Publicado: (2015)

Diabetes Care, Glycemic Control, Complications, and Concomitant Autoimmune Diseases in Children with Type 1 Diabetes in Turkey: A Multicenter Study
por: Şimşek, Damla Gökşen, et al.
Publicado: (2013)

Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children
por: Gökşen, Damla, et al.
Publicado: (2021)

Comparison of National Growth Standards for Turkish Infants and Children with World Health Organization Growth Standards
por: Bundak, Rüveyde, et al.
Publicado: (2022)

Two Siblings with Isolated GH Deficiency Due to Loss−of−Function Mutation in the GHRHR Gene: Successful Treatment with Growth Hormone Despite Late Admission and Severe Growth Retardation
por: Şıklar, Zeynep, et al.
Publicado: (2010)

Klinefelter Syndrome in Childhood: Variability in Clinical and Molecular Findings
por: Akcan, Neşe, et al.
Publicado: (2018)

A Critical Appraisal of Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome Patients in Turkey
por: Yavaş Abalı, Zehra, et al.
Publicado: (2016)

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study
por: Şıklar, Zeynep, et al.
Publicado: (2016)

Clinicopathological Characteristics of Papillary Thyroid Cancer in Children with Emphasis on Pubertal Status and Association with BRAFV600E Mutation
por: Poyrazoğlu, Şükran, et al.
Publicado: (2017)

Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity
por: Boyraz, Mehmet, et al.
Publicado: (2016)

Reply; Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene
por: Evliyaoğlu, Olcay
Publicado: (2016)

Children with chronic disease and COVID-19
por: Evliyaoğlu, Olcay
Publicado: (2020)

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism
por: Gürbüz, Fatih, et al.
Publicado: (2012)

Celiac Disease and Autoimmune Thyroid Disease in Children with Type 1 Diabetes Mellitus: Clinical and HLA−Genotyping Results
por: Ergür, Ayça Törel, et al.
Publicado: (2010)

Determination of insulin resistance and its relationship with hyperandrogenemia,anti-Müllerian hormone, inhibin A, inhibin B, and insulin-like peptide-3 levels in adolescent girls with polycystic ovary syndrome
por: YETİM ŞAHİN, Aylin, et al.
Publicado: (2019)

Combined Evaluation of IGF−1 and IGFBP−3 as an Index of Efficacy and Safety in Growth Hormone Treated Patients
por: Şıklar, Zeynep, et al.
Publicado: (2009)

Increased Carotid Intima-media Thickness and Its Association with Carbohydrate Metabolism and Adipocytokines in Children Treated with Recombinant Growth Hormone
por: Saygılı, Seha, et al.
Publicado: (2023)

Recommendations for Clinical Decision-making in Children with Type 1 Diabetes and Celiac Disease: Type 1 Diabetes and Celiac Disease Joint Working Group Report
por: Hatun, Şükrü, et al.
Publicado: (2022)

Multiple sulfatase deficiency: A case series of four children
por: Incecik, Faruk, et al.
Publicado: (2013)

Clinical Characteristics and Growth Hormone Treatment in Patients with Prader-Willi Syndrome
por: Dağdeviren Çakır, Aydilek, et al.
Publicado: (2021)

Severe Short Stature: an unusual finding in lipoid proteinosis
por: Poyrazoğlu, Şükran, et al.
Publicado: (2008)

Long-Term Endocrinologic Follow-Up of Children with Brain Tumors and Comparison of Growth Hormone Therapy Outcomes: A Single-Center Experience
por: Yavaş Abalı, Zehra, et al.
Publicado: (2023)

A Remarkable Coexistence of Systemic Capillary Leak Syndrome and Diabetes in an 11-Year-Old Boy: A Case Report and Review of the Literature
por: Ata, Aysun, et al.
Publicado: (2020)

The Impact of the CEDD-NET on the Evaluation of Rare Disorders: A Multicenter Scientific Research Platform in the Field of Pediatric Endocrinology
por: Özen, Samim, et al.
Publicado: (2022)

Is Premature Thelarche in the First Two Years of Life Transient?
por: Uçar, Ahmet, et al.
Publicado: (2012)

Reduced atherogenic indices in prepubertal girls with precocious adrenarche born appropriate for gestational age in relation to the conundrum of DHEAS
por: Uçar, Ahmet, et al.
Publicado: (2012)

Analysis of the caregiver burden associated with Sanfilippo syndrome type B: panel recommendations based on qualitative and quantitative data
por: Shapiro, Elsa, et al.
Publicado: (2019)

Coexistence of molybdenum cofactor deficiency type A and hypertrophic pyloric stenosis, a new case
por: Satar, Mehmet, et al.
Publicado: (2021)

Expert opinion on patient journey, diagnosis and clinical monitoring in acid sphingomyelinase deficiency in Turkey: a pediatric metabolic disease specialist's perspective
por: Arslan, Nur, et al.
Publicado: (2023)

Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene
por: Şahin, Sezgin, et al.
Publicado: (2017)

Effect of the COVID-19 quarantine on metabolic control in children and adolescents with type 1 diabetes
por: Turan, Hande, et al.
Publicado: (2022)

Effect of the COVID-19 quarantine on metabolic control in children and adolescents with type 1 diabetes
por: Turan, Hande, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_239vi27r2bseeb4tq3r5vjq1ui