Search Results - "Kizilcan Cetin, Sirmen"
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Mitotically Active Follicular Nodule in Early Childhood: A Case Report with a Novel Mutation in the Thyroglobulin Gene
Published in Journal of clinical research in pediatric endocrinology (01-09-2024)“…Dyshormonogenesis (DG) is the failure of thyroid hormone production due to a defect in thyroid hormonogenesis. Loss-of-function mutations in the thyroglobulin…”
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Evaluation of Abnormal Uterine Bleeding in Adolescents: Single Center Experience
Published in Journal of clinical research in pediatric endocrinology (01-09-2023)“…Abnormal uterine bleeding (AUB) is adolescent girls' most common gynecologic complaint. This study aimed to determine the diagnostic and management differences…”
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The Effect of Growth Hormone Therapy on Cardiac Outcomes in Noonan Syndrome: Long Term Follow-up Results
Published in Journal of clinical research in pediatric endocrinology (01-12-2022)“…Cardiac involvement is common in Noonan syndrome (NS). Concerns have been raised regarding the effect of recombinant growth hormone (rGH) use on ventricular…”
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Clinical Profile of Parathyroid Adenoma in Children and Adolescents: A Single-Center Experience
Published in Turkish archives of pediatrics (01-01-2023)“…Parathyroid adenoma is less common than in adulthood, but its morbidity is higher in children. We aimed to evaluate the clinical characteristics of parathyroid…”
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Clinical Characteristics and Treatment Outcomes of Children with Primary Osteoporosis
Published in Turkish archives of pediatrics (01-05-2023)“…Primary osteoporosis is a rare and essential problem in childhood that can cause severe skeletal deformities. We aimed to reveal the spectrum of primary…”
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Investigation of early puberty prevalence and time of addition thelarche to pubarche in girls with premature pubarche: two-year follow-up results
Published in Clinical Pediatric Endocrinology (2022)“…We aimed to determine the prevalence of early puberty in girls with premature pubarche and analyze the time interval between their pubarche and succeeding…”
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Recombinant GH treatment in a case of Costello syndrome with a 5-year follow-up
Published in Clinical Pediatric Endocrinology (01-01-2020)“…Costello syndrome (CS) is a rare member of the group of neuro-cardio-facio-cutaneous diseases known as RASopathies. CS involves characteristic dysmorphic…”
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Evaluation of aggression level in adolescent girls with classical congenital adrenal hyperplasia
Published in Clinical endocrinology (Oxford) (01-08-2023)“…Objective In patients with classical congenital adrenal hyperplasia (CAH), virilization affects the brain and external genitalia due to antenatal androgen…”
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Recombinant GH treatment in a case of Costello syndrome with a 5-year follow-up
Published in Clinical Pediatric Endocrinology (01-10-2020)“…[Abstract.] Costello syndrome (CS) is a rare member of the group of neuro-cardio-facio-cutaneous diseases known as RASopathies. CS involves characteristic…”
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Unraveling the Genetic Puzzle: Could MAP3K7 Be a Candidate Gene for RASopathies? Case Presentation
Published in Journal of clinical research in pediatric endocrinology (17-10-2024)“…Noonan Syndrome (NS) diagnosis is challenging due to diverse clinical manifestations. Here, our case report highlights 's novel role in NS. A 10.4-year-old…”
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Familial Clinical Heterogeneity of Medullary Thyroid Cancer with Germline RET S891A Protooncogene Mutation: 7-Year Follow-up with Successful Sorafenib Treatment
Published in Journal of clinical research in pediatric endocrinology (09-11-2023)“…Hereditary forms of Medullary thyroid carcinoma (MTC) are rare. Different phenotypes with the same mutation may be due to differences in the timing of RET…”
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Investigation of early puberty prevalence and time of addition thelarche to pubarche in girls with premature pubarche: two-year follow-up results
Published in Clinical Pediatric Endocrinology (2021)“…We aimed to determine the prevalence of early puberty in girls with premature pubarche and analyze the time interval between their pubarche and succeeding…”
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Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study
Published in Journal of clinical research in pediatric endocrinology (01-09-2024)“…Craniopharyngiomas (CPG) have complex treatment challenges due to their proximity to vital structures, surgical and radiotherapeutic complexities, and the…”
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Exploring Multiple Endocrinological Issues and Dysautonomia in a Rare Case: Hypoparathyroidism in MIRAGE Syndrome
Published in Journal of clinical research in pediatric endocrinology (26-03-2024)“…MIRAGE syndrome is a rare multisystemic disorder characterized by various manifestations, such as myelodysplasia, susceptibility to infections, growth…”
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Assessment of the Admission and Follow-up Characteristics of Children Diagnosed with Secondary Osteoporosis
Published in Journal of clinical research in pediatric endocrinology (02-07-2024)“…Secondary osteoporosis is a condition when the underlying disease or its treatment causes the bone mass to decrease and the bone structure to deteriorate,…”
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Evaluation of Growth Characteristics and Final Heights of Cases Diagnosed with Noonan Syndrome on GH Treatment
Published in Journal of clinical research in pediatric endocrinology (08-10-2024)“…Proportional short stature is one of the most important features of Noonan Syndrome, and adult height often remains below the 3rd percentile. Although the…”
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Pediatric Liver Transplantation Outcomes for Metabolic and Non-metabolic Diseases in Turkey: A Single Center Experience
Published in The journal of pediatric research (01-06-2019)“…Aim: Liver transplantation (LT) is performed for several indications in the pediatric population, including malignancy and acute hepatic failure among others…”
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Assessment of the Awareness of Prematurity and Related Problems
Published in The journal of pediatric research (01-12-2017)“…Aim: Prematurity is an important health problem affecting all segments of society. In this study, we aimed to evaluate the level of awareness of prematurity…”
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