Wissenschaftliche Arbeiten
Prof. Dr. Belma Haliloğlu
76 Publikationen. Neben jeder Publikation steht die Quelle der Angabe.
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Premature Pubarche, Hyperinsulinemia and Hypothyroxinemia: Novel Manifestations of Congenital Portosystemic Shunts (Abernethy Malformation) in Children
Hormone Research in Paediatrics, 2015
DOI 10.1159/000369395 PMID 25676144 24 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex
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Risk factors for mortality caused by hypothalamic obesity in children with hypothalamic tumours
Pediatric Obesity, 2015
DOI 10.1111/ijpo.12076 PMID 26463004 14 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex
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Growth without growth hormone syndrome in a patient with craniopharyngioma
JCRPE Journal of Clinical Research in Pediatric Endocrinology, 2015
1 Zitation (OpenAlex) Quelle: OpenAlex
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Factors Effecting Response to Growth Hormone Treatment in Children with Turner Syndrome
54th ESPE Meeting (ESPE 2015), 2015
Quelle: OpenAlex
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Hypothalamic obesity in children: pathophysiology to clinical management
Journal of Pediatric Endocrinology and Metabolism, 2015
DOI 10.1515/jpem-2014-0512 PMID 25781673 52 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex
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The Effectiveness of Sirolimus in a Newborn with Hyperinsulinaemic Hypoglycaemia
54th Annual ESPE, 2015
Quelle: OpenAlex
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Effects of leukemia inhibitory receptor gene mutations on human hypothalamo–pituitary–adrenal function
Pituitary, 2014
DOI 10.1007/s11102-014-0594-5 PMID 25145448 6 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex
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Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS
Bone, 2014
DOI 10.1016/j.bone.2014.10.006 PMID 25464124 25 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex
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Novel homozygous inactivating mutation of the calcium-sensing receptor gene (CASR) in neonatal severe hyperparathyroidism—lack of effect of cinacalcet
Bone, 2014
DOI 10.1016/j.bone.2014.04.010 PMID 24735972 30 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex
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Higher insulin detemir doses are required for the similar glycemic control: comparison of insulin detemir and glargine in children with type 1 diabetes mellitus
Pediatric Diabetes, 2014
DOI 10.1111/pedi.12167 PMID 25039448 16 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex
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Hypoglycemia: An unrecognized problem in cystic fibrosis (CF) patients unmasked by continues glucose monitorisation (CGM)
European Respiratory Journal, 2014
DOI 10.1183/13993003/erj.44.suppl_58.p1216 1 Zitation (OpenAlex) Quelle: OpenAlex
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Department of Pediatric Endocrinology, Marmara University
Dspace Repository (Marmara Üniversitesi), 2014
Quelle: OpenAlex
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Papillary Thyroid Cancer with Diffuse Pulmonary Metastasis: How to Manage?
53rd ESPE Meeting, 2014
Quelle: OpenAlex
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Eleven Years of Letrozole Treatment in a Child with 11-[beta] Hydroxylase Deficiency: Effect on Bone Age and Height Prognosis
53rd ESPE Meeting, 2014
Quelle: OpenAlex
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Sleep-related Breathing Disorders in Pycnodysostosis
53rd ESPE Meeting, 2014
Quelle: OpenAlex
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Is There a Change in the Presentation of Childhood Type-1 Diabetes Mellitus in the Last 15 Years? Data from a Tertiary Care Center in Turkey
ESPE 2014, 2014
Quelle: OpenAlex
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Hyperthyroidism Due to TSH Secreting Pituitary Adenoma in a 7-Year-Old Boy
53rd ESPE Meeting, 2014
Quelle: OpenAlex
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GAD Antibody Positivity is Associated with Higher Prevalence of Autoimmune Thyroiditis in Children with Type 1 Diabetes Mellitus
53rd ESPE Meeting, 2014
Quelle: OpenAlex
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Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features
Orphanet Journal of Rare Diseases, 2014
DOI 10.1186/1750-1172-9-60 PMID 24767306 31 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex
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Sleep disordered breathing in pycnodysostosis patients
European Respiratory Journal, 2014
DOI 10.1183/13993003/erj.44.suppl_58.p2277 1 Zitation (OpenAlex) Quelle: OpenAlex
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Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia
European Journal of Pediatrics, 2012
DOI 10.1007/s00431-012-1868-4 PMID 23093139 7 Zitationen (Europe PMC) Frei zugänglicher VolltextQuelle: OpenAlex
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An Atypical Case of Familial Glucocorticoid Deficiency without Pigmentation Caused by Coexistent Homozygous Mutations inMC2R(T152K) andMC1R(R160W)
The Journal of Clinical Endocrinology & Metabolism, 2012
DOI 10.1210/jc.2011-2414 PMID 22337906 31 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex
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A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo-cardiomyopathy
Gene, 2012
DOI 10.1016/j.gene.2012.11.044 PMID 23235116 20 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex
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Complementary and Alternative Medicine in Children with Type 1 Diabetes Mellitus
Journal of Clinical Research in Pediatric Endocrinology, 2011
DOI 10.4274/jcrpe.v3i3.27 PMID 21911327 22 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex
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Ensefalopati Tablosuyla Gelen Leigh Sendromu
Çocuk Dergisi / Journal of Child, 2010
DOI 10.5222/j.child.2010.094 2 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex
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Karbon monoksit zehirlenmesine bağlı ciddi geç nörotoksisite: Vaka sunumu
Çanakkale Onsekiz Mart University AVESIS, 2007
Quelle: OpenAlex