Results 131 to 140 of about 71,302 (277)

Empty sella Syndrome as a Cause of Hypopituitarism Case study

open access: yesDiyala Journal of Medicine, 2018
Background:Empty sella syndrome is the radiological appearance of an enlarged or deformed sella turcica which is partially or completely filled with cerebrospinal fluid .In 20-50% of patients there may be endocrinologic dysfunction, pan hypopituitarism ...
Yousif Baha'addin Ahmed
doaj   +2 more sources

Management of a Girl With Delayed Puberty and Elevated Gonadotropins. [PDF]

open access: yesJ Endocr Soc, 2022
McGlacken-Byrne SM   +2 more
europepmc   +1 more source

Clinical Challenges in Transition to Adult Care for Young People With Endocrinopathies

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT The complexity of transition of pediatric patients to adult care is well recognized, with a multidisciplinary approach widely agreed to be essential. Despite extensive existing literature in this area, practical guidance as to the management of specific medical aspects and how to address these with patients and families is lacking, with little
Margaret Zacharin, Quynh‐Nhu Nguyen
wiley   +1 more source

Spectrum of Hypogonadism and Its Management in Adolescents With Prader‐Willi Syndrome: A Retrospective Cohort Study Over 35 Years

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Context Adult data indicate that hypogonadism is underdiagnosed and undertreated in Prader‐Willi Syndrome (PWS). Objectives We aimed to describe the spectrum of pubertal development, and the diagnosis and treatment of hypogonadism in paediatric/adolescent patients with PWS. Design/Patients A retrospective cohort study of patients with PWS aged
Helen Nguyen   +2 more
wiley   +1 more source

Diagnosis of Growth Hormone Deficiency in Children: Comparative Performance of Arginine Versus Glucagon as the First Stimulation Test

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Objective Growth hormone deficiency (GHD) diagnosis typically requires the performance of two sequential stimulation tests. Glucagon stimulation test (GST) and arginine stimulation test (AST) are widely used. This study aimed to determine the most suitable order of tests.
David Shaki   +6 more
wiley   +1 more source

Genetic, epigenetic and enviromental influencing factors on the regulation of precocious and delayed puberty. [PDF]

open access: yesFront Endocrinol (Lausanne), 2022
Faienza MF   +5 more
europepmc   +1 more source

Comparing Foster and Non‐Foster Adolescents: A Pilot Study on Relationships and Psychological Difficulties

open access: yesChild &Family Social Work, EarlyView.
ABSTRACT Adolescents experience substantial changes in their close relationships, which are linked to psychological adjustment. Research on relationships among adolescents in foster care is limited, especially in Germany. This pilot study (N = 30; 15 in foster families, 15 in biological families) explored how relationship qualities—measured by the ...
Julia Festini   +2 more
wiley   +1 more source

Treatment of constitutional delayed puberty with a combination of testosterone esters

open access: yesThe Turkish Journal of Pediatrics, 1993
Thirteen boys with constitutional delayed puberty (CDP) were treated with a combination of short and long-acting testosterone esters (testosterone propionate, testosterone phenylpropionate, testosterone isocaproate).
A Büyükgebiz
doaj  

Functional Data Strengthen Clinical Validation of PhenoScore Phenotype‐Guided AI for ANKRD11 Missense Variants

open access: yesClinical Genetics, EarlyView.
PhenoScore, an AI framework integrating facial recognition and clinical phenotype data, accurately identifies pathogenic ANKRD11 missense variants associated with KBG syndrome (AUC 0.95). Validated against functional data, PhenoScore outperforms REVEL and complements AlphaMissense, providing objective phenotypic evidence to reduce variants of uncertain
Evi Andriessen   +5 more
wiley   +1 more source

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