B. Yüksel

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Inactivating KISS1 Mutation and Hypogonadotropic Hypogonadism

L. D. Kotan, F. Gurbuz, R. Millar, 2012 .

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

F. Baş, F. Darendeliler, F. Demirel, 2016, American journal of medical genetics. Part A.

Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study

S. Poyrazoglu, F. Baş, F. Darendeliler, 2015, Journal of clinical research in pediatric endocrinology.

The first report of cabergoline-induced immune hemolytic anemia in an adolescent with prolactinoma

B. Yüksel, Fatih Gürbüz, B. Yağcı-Küpeli, 2014, Journal of pediatric endocrinology & metabolism : JPEM.

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group

F. Baş, F. Darendeliler, F. Demirel, 2015, Journal of clinical research in pediatric endocrinology.

DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism

A. Topaloğlu, L. D. Kotan, E. Mengen, 2021, Hormone Research in Paediatrics.

Serum IL-1, IL-2, TNFalpha and INFgamma levels of patients with type 1 diabetes mellitus and their siblings.

A. Topaloğlu, B. Yüksel, N. Onenli-Mungan, 2003, Journal of pediatric endocrinology & metabolism : JPEM.

Gender Identity and Assignment Recommendations in Disorders of Sex Development Patients: 20 Years’ Experience and Challenges

A. Topaloğlu, Gonca Çelik, B. Yüksel, 2020, Journal of clinical research in pediatric endocrinology.

Neuroendocrinological Control of Obesity

B. Yüksel, 2009 .

Pulmonary hypertension, heart failure and neutropenia due to diazoxide therapy

M. Yilmaz, B. Yüksel, D. Yıldızdaş, 2008, Advances in therapy.

Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey

M. Yılmaz, S. Balcı, B. Yüksel, 2018, Journal of clinical research in pediatric endocrinology.

Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1

I. Carr, A. Topaloğlu, L. D. Kotan, 2016, Journal of clinical research in pediatric endocrinology.

Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia

A. Öztürk, S. Poyrazoglu, F. Baş, 2020, Journal of clinical research in pediatric endocrinology.

Thyroid Hormone Levels and their Relationship to Survival in Children with Bacterial Sepsis and Septic Shock

Y. Sertdemir, B. Yüksel, D. Yıldızdaş, 2004 .

Clinical features of Bardet‐Biedl syndrome

B. Yüksel, E. Alhan, N. Demircan, 1995, Acta paediatrica Japonica : Overseas edition.

Growth hormone and insulin‐like growth factor 1 levels and their relation to survival in children with bacterial sepsis and septic shock

B. Yüksel, D. Yıldızdaş, H. Yapıcıoğlu, 2004, Journal of paediatrics and child health.

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

F. Darendeliler, N. Mungan, A. Bideci, 2011, Journal of clinical research in pediatric endocrinology.

Unusual and early onset IPEX syndrome: a case report.

M. Yılmaz, B. Yüksel, D. Altintas, 2019, The Turkish journal of pediatrics.

Serum IL-1, IL-2, TNFα and INFγ Levels of Patients with Type 1 Diabetes Mellitus and their Siblings

B. Yüksel, M. Yılmaz, S. Çetiner, 2003 .

A case of ambiguous genitalia with unilateral amelia and unilateral peromelia of the upper limbs

B. Yüksel, R. Tuncer, Ünal Zorludemir, 1997, Acta paediatrica Japonica : Overseas edition.

Congenital lipoid adrenal hyperplasia: functional characterization of three novel mutations in the STAR gene.

S. Bens, I. Leuschner, A. Mohn, 2010, The Journal of clinical endocrinology and metabolism.

The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development

J. Grötzinger, A. Topaloğlu, E. Mengen, 2013, Hormone Research in Paediatrics.

Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study

F. Baş, F. Darendeliler, Z. Aycan, 2015, Endocrine.

Changes in the presentation of newly diagnosed type 1 diabetes in children during the COVID-19 pandemic in a tertiary center in Southern Turkey

B. Yüksel, Fatih Gürbüz, Ihsan Turan, 2021, Journal of pediatric endocrinology & metabolism : JPEM.

Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency

E. Mengen, B. Yüksel, Fatih Gürbüz, 2020, Journal of clinical research in pediatric endocrinology.

IgG subclass levels in patients with Down's syndrome

B. Yüksel, D. Altintas, S. Güneşer, 1996 .

Epidemiology of meningococcal infections in children in mid-southern part of Turkey

B. Yüksel, E. Alhan, N. Bozdemir, 1995, European Journal of Epidemiology.

Tuberculous meningitis in children

B. Yüksel, E. Alhan, Ş. Altunbaşak, 1994, Acta paediatrica Japonica : Overseas edition.

Fucosidosis with hypothyroidism: a case report.

G. Besley, A. Topaloğlu, B. Yüksel, 2004, The Turkish journal of pediatrics.

Idiopathic hyperphosphatasia and TNFRSF11B mutations: relationships between phenotype and genotype.

J. Kanis, M. Hegde, B. Tüysüz, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype

J. Kanis, M. Hegde, B. Tüysüz, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Type II hyperprolinemia: a case report.

A. Topaloğlu, B. Yüksel, N. Onenli-Mungan, 2004, The Turkish journal of pediatrics.

21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplification.

L. D. Kotan, F. Gurbuz, B. Yüksel, 2020, European journal of medical genetics.

Impaired glucose tolerance in Fanconi-Bickel syndrome: Eight patients with two novel mutations.

A. Topaloğlu, B. Yüksel, D. Kör, 2017, The Turkish journal of pediatrics.

Efficiency of Single Dose of Tolvaptan Treatment During the Triphasic Episode After Surgery for Craniopharyngioma

B. Yüksel, Fatih Gürbüz, Ihsan Turan, 2018, Journal of clinical research in pediatric endocrinology.

Evaluation of Permanent Growth Hormone Deficiency (GHD) in Young Adults with Childhood Onset GHD: A multicenter study

S. Poyrazoglu, F. Darendeliler, A. Bideci, 2008, Journal of clinical research in pediatric endocrinology.

Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

S. Poyrazoglu, F. Darendeliler, S. Kurtoğlu, 2015, Journal of clinical research in pediatric endocrinology.

Membranoproliferative glomerulonephritis associated with insulin-dependent diabetes mellitus. A case report.

A. Anarat, B. Yüksel, A. Noyan, 1996, Nephron.

Early onset of diabetic nephropathy in a child with type 1 diabetes mellitus.

A. Anarat, B. Yüksel, A. Noyan, 2003, The Turkish journal of pediatrics.

Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations

A. Topaloğlu, L. D. Kotan, E. Mengen, 2017, Journal of clinical research in pediatric endocrinology.

Novel Growth Hormone Receptor Gene Mutation in a Patient with Laron Syndrome

A. Topaloğlu, F. Temiz, B. Yüksel, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Coexistence of Kabuki Syndrome and Autoimmune Thyroiditis

A. Topaloğlu, B. Yüksel, Fatih Gürbüz, 2016, Journal of clinical research in pediatric endocrinology.

Vitamin D Deficiency in Obsessive-Compulsive Disorder Patients with Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infections: A Case Control Study.

B. Yüksel, A. Tahiroglu, A. Avcı, 2016, Noro psikiyatri arsivi.

ARAŞTIRMA/RESEARCH Neurological assessment of 38 late-diagnosed children with classic phenylketonuria

B. Yüksel, A. Kemal, G. Özer, 2016 .

Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

S. Poyrazoglu, A. Topaloğlu, L. D. Kotan, 2012, Journal of Clinical Research in Pediatric Endocrinology.

Genotypic and phenotypic features of the cystinosis patients from the South Eastern part of Turkey.

N. Cengiz, A. Anarat, A. Topaloğlu, 2016, The Turkish journal of pediatrics.

Efficiency of Single Dose of Tolvaptan Treatment During the Triphasic Episode After Surgery for Craniopharyngioma

B. Yüksel, Fatih Gürbüz, Ihsan Turan, 2018, Journal of clinical research in pediatric endocrinology.

Short stature and insulin-like growth Factor-I in neurofibromatosis Type I

B. Yüksel, F. Incecik, Ş. Altunbaşak, 2021, Annals of Medical Research.

Neurokinin B Signalling in Human Puberty

A. Topaloğlu, L. D. Kotan, B. Yuksel, 2010, Journal of neuroendocrinology.

Relationship between metabolic control and neurocognitive functions in children diagnosed with type I diabetes mellitus before and after 5 years of age.

A. Topaloğlu, F. Temiz, B. Yüksel, 2012, The Turkish journal of pediatrics.

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation

A. Topaloğlu, B. Yüksel, Fatih Gürbüz, 2016, Journal of clinical research in pediatric endocrinology.

Congenital lipoid adrenal hyperplasia: functional characterization of three novel mutations in the STAR gene.

S. Bens, I. Leuschner, A. Mohn, 2010, The Journal of clinical endocrinology and metabolism.

“Different Clinical Effects of Ectodermal Dysplasias in Four Generations

O. Demirhan, B. Yüksel, S. Yilmaz, 2023, Actas dermo-sifiliograficas.

Idiopathic Hyperphosphatasia and TNFRSF11B Mutations: Relationships Between Phenotype and Genotype

J. Kanis, M. Hegde, B. Tüysüz, 2003, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.