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The Genetic Landscape of Children Born Small for Gestational Age with Persistent Short Stature
The Genetic Landscape of Children Born Small for Gestational Age with Persistent Short Stature
<b><i>Introduction:</i></b> Among children born small for gestational age, 10–15% fail to catch up...
Glycemic control by treatment modalities: national registry-based population data in children and adolescents with type 1 diabetes
Glycemic control by treatment modalities: national registry-based population data in children and adolescents with type 1 diabetes
AIMS To assess the differences in key parameters of type 1 diabetes (T1D) control associated with treatment and monitoring...
KEY STAGES IN THE DEVELOPMENT AND ESTABLISHMENT OF PAEDIATRIC ENDOCRINOLOGY - A TEMPLATE FOR FUTURE PROGRESS
KEY STAGES IN THE DEVELOPMENT AND ESTABLISHMENT OF PAEDIATRIC ENDOCRINOLOGY - A TEMPLATE FOR FUTURE PROGRESS
Background Paediatric endocrinology became recognised in Western European countries in the 1960s and 1970s. It is now a th...
Hormone Replacement Therapy After Pubertal Induction in Adolescents and Young Adults with Turner Syndrome: A Survey Study.
Hormone Replacement Therapy After Pubertal Induction in Adolescents and Young Adults with Turner Syndrome: A Survey Study.
Introduction: Turner syndrome (TS) is associated with primary ovarian insufficiency (POI) and most adolescents and young a...
A critical review of upcoming new therapeutic options in paediatric endocrinology
A critical review of upcoming new therapeutic options in paediatric endocrinology
Novel and innovative therapeutic options are now available or will soon become available for treating children and adolesc...
Effect of Growth Hormone Therapy on Pubertal Timing: Systematic Review and Meta-analysis
Effect of Growth Hormone Therapy on Pubertal Timing: Systematic Review and Meta-analysis
Introduction Recombinant human growth hormone (rhGH) therapy effectively increases height in various disorders of childhoo...
Assessment of nutritional status in the diagnostic evaluation of the child with growth failure
Assessment of nutritional status in the diagnostic evaluation of the child with growth failure
Current clinical guidelines provide information about the diagnostic work-up of children with growth failure. This mini-re...
Growth hormone dose modulation and final height in short children born small for gestational age: French real-life data
Growth hormone dose modulation and final height in short children born small for gestational age: French real-life data
Introduction Growth hormone (GH) therapy improves height outcomes in short children born small for gestational age (SGA); ...
Improvements in glucose regulation in children and young people with cystic fibrosis related diabetes following initiation of Elexacaftor/Tezacaftor/Ivacaftor
Improvements in glucose regulation in children and young people with cystic fibrosis related diabetes following initiation of Elexacaftor/Tezacaftor/Ivacaftor
Introduction: Cystic fibrosis transmembrane receptor (CFTR) modulators are increasingly used in children and young people ...
The genetic landscape of children born small for gestational age with persistent short stature (SGA-SS)
The genetic landscape of children born small for gestational age with persistent short stature (SGA-SS)
Introduction. Among children born small for gestational age, 10-15% fails to catch-up and remains short (SGA-SS). The und...
Why should orchidopexy be performed in congenital hypogonadotropic hypogonadism, and when?
Why should orchidopexy be performed in congenital hypogonadotropic hypogonadism, and when?
Background: In otherwise normal boys with undescended testes, early orchidopexy is recommended to preserve fertility, to d...
Weekly Growth Hormone (Lonapegsomatropin) Causes Severe Transient Hyperglycemia in a Child with Obesity
Weekly Growth Hormone (Lonapegsomatropin) Causes Severe Transient Hyperglycemia in a Child with Obesity
Abstract Introduction: A 12-year-9-month-old non-Hispanic black male with a history of growth hormone deficiency (GHD), pi...
Molecular genetic analysis and growth hormone treatment in a three-generation Chinese family with Tricho-rhino-phalangeal syndrome I
Molecular genetic analysis and growth hormone treatment in a three-generation Chinese family with Tricho-rhino-phalangeal syndrome I
Background: Tricho-rhino-phalangeal syndrome (TRPS) is a rare genetic disorder characterized by craniofacial and skeletal ...
Reversible hypothalamic obesity in a girl with suprasellar tuberculoma
Reversible hypothalamic obesity in a girl with suprasellar tuberculoma
Introduction: Suprasellar tuberculoma are extremely rare in children and most of those patients present with headache, vom...
The effects of five years of growth hormone treatment on growth and body composition in patients with Temple syndrome
The effects of five years of growth hormone treatment on growth and body composition in patients with Temple syndrome
Introduction: Temple syndrome (TS14) is a rare imprinting disorder caused by maternal uniparental disomy of chromosome 14 ...
An Overlooked Manifestation of Hypercortisolism - Cerebral Cortical Atrophy and Challenges in Identifying the Etiology of Hypercortisolism: A Report of 2 Pediatric Cases
An Overlooked Manifestation of Hypercortisolism - Cerebral Cortical Atrophy and Challenges in Identifying the Etiology of Hypercortisolism: A Report of 2 Pediatric Cases
Introduction: Endogenous Cushing’s syndrome (CS) is a rare, severe disease that can cause multiple systemic involvement an...
Author Index Vol. 96, No. 1, 2023
Author Index Vol. 96, No. 1, 2023
Hormone Resea...
Subject Index Vol. 96, No. 1, 2023
Subject Index Vol. 96, No. 1, 2023
Hormone Resea...
11th International Meeting of Paediatric Endocrinology (IMPE) - Abstracts
11th International Meeting of Paediatric Endocrinology (IMPE) - Abstracts
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XXX Annual Meeting of the Latin American Pediatric Endocrinology Society (SLEP) Bogota, Colombia, October 19-22, 2022
XXX Annual Meeting of the Latin American Pediatric Endocrinology Society (SLEP) Bogota, Colombia, October 19-22, 2022
XXX Annual Meeting of the Latin American Pediatric Endocrinology Society (SLEP) Bogota, Colombia, October 19–22, 2022
Novel Calcium-Sensing Receptor (CASR) Mutation in a Family with Autosomal Dominant Hypocalcemia Type 1 (ADH1): Genetic Study over Three Generations and Clinical Characteristics
Novel Calcium-Sensing Receptor (CASR) Mutation in a Family with Autosomal Dominant Hypocalcemia Type 1 (ADH1): Genetic Study over Three Generations and Clinical Characteristics
Introduction: Activating mutation of the calcium-sensing receptor gene (CASR) reduces parathyroid hormone secretion and re...
Compromised adult height in females with non-classical congenital adrenal hyperplasia diagnosed in childhood
Compromised adult height in females with non-classical congenital adrenal hyperplasia diagnosed in childhood
Introduction Data on adult height (AHt) in individuals with non-classical congenital adrenal hyperplasia (NCCAH) are incon...
Review of implant gonadotrophin-releasing hormone agonist use: experience in a single academic center
Review of implant gonadotrophin-releasing hormone agonist use: experience in a single academic center
Background: Gonadotrophin-releasing hormone agonists (GnRHa) are used for puberty suppression in central precocious pubert...
Rhabdomyolysis: A rare presentation of Hashimoto thyroiditis in an adolescent boy and review of the literature
Rhabdomyolysis: A rare presentation of Hashimoto thyroiditis in an adolescent boy and review of the literature
Introduction: Hypothyroidism-induced rhabdomyolysis without precipitating factors is extremely rare, particularly in pedia...
Subtotal Parathyroidectomy Successfully Controls Calcium Levels of Patients with Neonatal Severe Hyperparathyroidism Carrying a Novel CASR Mutation
Subtotal Parathyroidectomy Successfully Controls Calcium Levels of Patients with Neonatal Severe Hyperparathyroidism Carrying a Novel CASR Mutation
<b><i>Introduction:</i></b> Inactivating mutations of the calcium-sensing receptor (<i>CASR&...
Infants with Congenital Adrenal Hyperplasia Exhibit Thalamic Discrepancies in Early Brain Structure
Infants with Congenital Adrenal Hyperplasia Exhibit Thalamic Discrepancies in Early Brain Structure
Introduction: Patients with classical congenital adrenal hyperplasia (CAH) have prenatal and postnatal hormonal imbalances...
Patient and parent perspectives on testicular adrenal rest tumors in congenital adrenal hyperplasia
Patient and parent perspectives on testicular adrenal rest tumors in congenital adrenal hyperplasia
Background: Testicular adrenal rest tumors (TARTs) increase the risk of infertility in males with classic congenital adre...
Raised Thyroid Stimulating Hormone in Girls with Polycystic Ovary Syndrome: Effects of Randomized Interventions
Raised Thyroid Stimulating Hormone in Girls with Polycystic Ovary Syndrome: Effects of Randomized Interventions
Introduction Polycystic ovary syndrome (PCOS) in women associates with raised levels of circulating thyroid stimulating ho...
Adrenal Insufficiency in Peroxisomal Disorders: a Single Institution Case Series
Adrenal Insufficiency in Peroxisomal Disorders: a Single Institution Case Series
Introduction: There are two major categories of peroxisomal disorders (PD): Peroxisomal biogenesis disorders (PBD) due to ...
Five-Year Therapy with Recombinant Human Insulin-Like Growth Factor-1 in a Patient with PAPP-A2 Deficiency
Five-Year Therapy with Recombinant Human Insulin-Like Growth Factor-1 in a Patient with PAPP-A2 Deficiency
Introduction: The metalloproteinase pregnancy-associated plasma protein A2 (PAPP-A2) cleaves insulin-like growth factor (I...
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