受强制性开放获取政策约束的文章 - khalid Hussain了解详情
无法在其他位置公开访问的文章：18 篇
Neonatal hypoglycemia
VB Arya, S Senniappan, M Guemes, K Hussain
The Indian Journal of Pediatrics 81, 58-65, 2014
强制性开放获取政策： UK Medical Research Council
18F-DOPA PET and enhanced CT imaging for congenital hyperinsulinism: initial UK experience from a technologist’s perspective
M Meintjes, R Endozo, J Dickson, K Erlandsson, K Hussain, C Townsend, ...
Nuclear Medicine Communications 34 (6), 601-608, 2013
强制性开放获取政策： UK Medical Research Council
Insulinoma in childhood: clinical, radiological, molecular and histological aspects of nine patients
R Padidela, M Fiest, V Arya, VV Smith, M Ashworth, D Rampling, ...
European journal of endocrinology 170 (5), 741-747, 2014
强制性开放获取政策： UK Medical Research Council, Wellcome Trust
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
Prospective study in bullous pemphigoid: association of high serum anti‐BP180 IgG levels with increased mortality and reduced Karnofsky score
MM Holtsche, S Goletz, N van Beek, D Zillikens, S Benoit, K Harman, ...
British Journal of Dermatology 179 (4), 918-924, 2018
强制性开放获取政策： German Research Foundation, National Institute for Health Research, UK
Sirolimus therapy in a patient with severe hyperinsulinaemic hypoglycaemia due to a compound heterozygous ABCC8 gene mutation
P Shah, VB Arya, SE Flanagan, K Morgan, S Ellard, S Senniappan, ...
Journal of Pediatric Endocrinology and Metabolism 28 (5-6), 695-699, 2015
强制性开放获取政策： UK Medical Research Council, Wellcome Trust
Pediatric hypoglycemia
TF Lang, K Hussain
Advances in clinical chemistry 63, 211-245, 2014
强制性开放获取政策： UK Medical Research Council
Protein-induced hyperinsulinaemic hypoglycaemia due to a homozygous HADH mutation in three siblings of a Saudi family
O Babiker, SE Flanagan, S Ellard, HA Girim, K Hussain, S Senniappan
Journal of Pediatric Endocrinology and Metabolism 28 (9-10), 1073-1077, 2015
强制性开放获取政策： Wellcome Trust
Biochemical studies in patients with hyperinsulinaemic hypoglycaemia
H Al-Otaibi, S Senniappan, S Alam, K Hussain
European journal of pediatrics 172, 1435-1440, 2013
强制性开放获取政策： UK Medical Research Council
Diazoxide toxicity in a child with persistent hyperinsulinemic hypoglycemia of infancy: mixed hyperglycemic hyperosmolar coma and ketoacidosis
P Mangla, K Hussain, S Ellard, SE Flanagan, V Bhatia
Journal of Pediatric Endocrinology and Metabolism 31 (8), 943-945, 2018
强制性开放获取政策： Wellcome Trust, Royal Society UK
The heterogeneity of hyperinsulinaemic hypoglycaemia in 19 patients with Beckwith-Wiedemann syndrome due to KvDMR1 hypomethylation
S Senniappan, D Ismail, C Shipster, C Beesley, K Hussain
Journal of Pediatric Endocrinology and Metabolism 28 (1-2), 83-86, 2015
强制性开放获取政策： UK Medical Research Council
Sirolimus precipitating diabetes mellitus in a patient with congenital hyperinsulinaemic hypoglycaemia due to autosomal dominant ABCC8 mutation
A Dastamani, M Güemes, J Walker, P Shah, K Hussain
Journal of Pediatric Endocrinology and Metabolism 30 (11), 1219-1222, 2017
强制性开放获取政策： UK Medical Research Council
Paradoxical hypoglycaemia associated with diazoxide therapy for hyperinsulinaemic hypoglycaemia
C Ponmani, H Gannon, K Hussain, S Senniappan
Hormone Research in Paediatrics 80 (2), 129-133, 2013
强制性开放获取政策： UK Medical Research Council
Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation
X Su, Y Feng, SA Rahman, S Wu, G Li, F Rüschendorf, L Zhao, H Cui, ...
Journal of Genetics and Genomics 47 (10), 618-626, 2020
强制性开放获取政策： 国家自然科学基金委员会, German Research Foundation
Neonatal diabetes in an infant of diabetic mother: Same novel INS missense mutation in the mother and her offspring
MA Ozturk, S Kurtoglu, O Bastug, L Korkmaz, G Daar, S Memur, H Halis, ...
Journal of Pediatric Endocrinology and Metabolism 27 (7-8), 745-748, 2014
强制性开放获取政策： UK Medical Research Council, Wellcome Trust
Congenital hyperinsulinism, neonatal diabetes and the risk of malignancies: an international collaborative study. Preliminary communication.
M Makov, G Chodick, K Mohnike, T Otonkoski, H Huopio, I Banerjee, ...
Diabetic Medicine 32 (5), 2015
强制性开放获取政策： UK Medical Research Council
Clinical presentation and treatment response to diazoxide in two siblings with congenital hyperinsulinism as a result of a novel compound heterozygous ABCC8 missense mutation
S Galcheva, V Iotova, S Ellard, SE Flanagan, I Halvadzhiyan, C Petrova, ...
Journal of Pediatric Endocrinology and Metabolism 30 (4), 471-474, 2017
强制性开放获取政策： UK Medical Research Council, Wellcome Trust
Hypopituitarism in a patient with Beckwith-Wiedemann syndrome due to hypomethylation of KvDMR1
M Baiocchi, FS Yousuf, K Hussain
Pediatrics 133 (4), e1082-e1086, 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：73 篇
Recommendations from the pediatric endocrine society for evaluation and management of persistent hypoglycemia in neonates, infants, and children
PS Thornton, CA Stanley, DD De Leon, D Harris, MW Haymond, ...
The Journal of pediatrics 167 (2), 238-245, 2015
强制性开放获取政策： US National Institutes of Health
Insulin Mutation Screening in 1,044 Patients With Diabetes: Mutations in the INS Gene Are a Common Cause of Neonatal Diabetes but a Rare Cause of Diabetes …
EL Edghill, SE Flanagan, AM Patch, C Boustred, A Parrish, B Shields, ...
Diabetes 57 (4), 1034-1042, 2008
强制性开放获取政策： US National Institutes of Health
出版信息和资助信息由计算机程序自动确定