受强制性开放获取政策约束的文章 - Huseyin Demirbilek了解详情
无法在其他位置公开访问的文章：1 篇
Persistent hyperinsulinaemic hypoglycaemia in infancy
P Shah, H Demirbilek, K Hussain
Seminars in Pediatric Surgery 23 (2), 76-82, 2014
强制性开放获取政策： UK Medical Research Council
可在其他位置公开访问的文章：14 篇
Rare causes of primary adrenal insufficiency: genetic and clinical characterization of a large nationwide cohort
T Guran, F Buonocore, N Saka, MN Ozbek, Z Aycan, A Bereket, F Bas, ...
The Journal of Clinical Endocrinology & Metabolism 101 (1), 284-292, 2016
强制性开放获取政策： National Institute for Health Research, UK, Wellcome Trust
Congenital hyperinsulinism: diagnosis and treatment update
H Demirbilek, K Hussain
Journal of clinical research in pediatric endocrinology 9 (Suppl 2), 69, 2017
强制性开放获取政策： UK Medical Research Council
Pancreatic endocrine and exocrine function in children following near-total pancreatectomy for diffuse congenital hyperinsulinism
VB Arya, S Senniappan, H Demirbilek, S Alam, SE Flanagan, S Ellard, ...
PloS one 9 (5), e98054, 2014
强制性开放获取政策： UK Medical Research Council
Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations
H Demirbilek, VB Arya, MN Ozbek, JAL Houghton, RT Baran, M Akar, ...
European Journal of Endocrinology 172 (6), 697-705, 2015
强制性开放获取政策： Diabetes UK, UK Medical Research Council, National Institute for Health …
Long-term follow-up of children with congenital hyperinsulinism on octreotide therapy
H Demirbilek, P Shah, VB Arya, L Hinchey, SE Flanagan, S Ellard, ...
The Journal of Clinical Endocrinology & Metabolism 99 (10), 3660-3667, 2014
强制性开放获取政策： UK Medical Research Council, Wellcome Trust
Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability
A Raimondo, AJ Chakera, SK Thomsen, K Colclough, A Barrett, ...
Human molecular genetics 23 (24), 6432-6440, 2014
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
Clinical and hormonal profiles correlate with molecular characteristics in patients with 11β-hydroxylase deficiency
M Yildiz, E Isik, ZY Abali, M Keskin, MN Ozbek, F Bas, SA Ucakturk, ...
The Journal of Clinical Endocrinology & Metabolism 106 (9), e3714-e3724, 2021
强制性开放获取政策： UK Medical Research Council
Permanent neonatal diabetes mellitus and neurological abnormalities due to a novel homozygous missense mutation in NEUROD1
H Demirbilek, N Hatipoglu, U Gul, ZU Tatli, S Ellard, SE Flanagan, ...
Pediatric diabetes 19 (5), 898-904, 2018
强制性开放获取政策： Wellcome Trust, Royal Society UK
Clinical characteristics and phenotype–genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations
H Demirbilek, VB Arya, MN Ozbek, A Akinci, M Dogan, F Demirel, ...
European journal of endocrinology 170 (6), 885-892, 2014
强制性开放获取政策： UK Medical Research Council
Congenital hyperinsulinism and evolution to Sulfonylurearesponsive diabetes later in life due to a novel homozygous p. L171F ABCC8 Mutation
E Işık, H Demirbilek, JA Houghton, S Ellard, SE Flanagan, K Hussain
Journal of clinical research in pediatric endocrinology 11 (1), 82, 2019
强制性开放获取政策： UK Medical Research Council
Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics
KA Patel, MN Ozbek, M Yildiz, T Guran, C Kocyigit, S Acar, Z Siklar, M Atar, ...
Diabetologia, 1-7, 2022
强制性开放获取政策： National Institute for Health Research, UK, Wellcome Trust, Royal Society UK
Familial isolated growth hormone deficiency due to a novel homozygous missense mutation in the growth hormone releasing hormone receptor gene: clinical presentation with …
H Demirbilek, S Tahir, RT Baran, M Sherif, P Shah, MN Ozbek, ...
The Journal of Clinical Endocrinology & Metabolism 99 (12), E2730-E2734, 2014
强制性开放获取政策： UK Medical Research Council
Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations
H Demirbilek, A Cayir, SE Flanagan, R Yıldırım, Y Kor, F Gurbuz, ...
The Journal of Clinical Endocrinology & Metabolism 105 (12), e4351-e4359, 2020
强制性开放获取政策： Diabetes UK, National Institute for Health Research, UK, Wellcome Trust …
Perinatal hypophosphatasia in a premature infant
D Sankaran, PK Chandrasekharan, M Rawat
American Journal of Perinatology Reports 10 (02), e139-e147, 2020
强制性开放获取政策： US National Institutes of Health
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