Published in Indian J Endocrinol Metab on October 01, 2013
Study of awareness of adrenal disorders among interns and postgraduate students of Hamidia Hospital, Bhopal. Indian J Endocrinol Metab (2017) 0.75
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab (2010) 3.80
Consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology. J Clin Endocrinol Metab (2002) 2.97
Clinical review: Adult height in patients with congenital adrenal hyperplasia: a systematic review and metaanalysis. J Clin Endocrinol Metab (2010) 1.47
Testicular adrenal rest tumours in congenital adrenal hyperplasia. Best Pract Res Clin Endocrinol Metab (2009) 1.39
Health problems in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Horm Res Paediatr (2011) 1.29
Approach to the patient: the adult with congenital adrenal hyperplasia. J Clin Endocrinol Metab (2013) 1.10
Unfavourable trends in cardiovascular and metabolic risk in paediatric and adult patients with congenital adrenal hyperplasia? Clin Endocrinol (Oxf) (2009) 0.97
Bone mineral density, bone markers, and fractures in adult males with congenital adrenal hyperplasia. Eur J Endocrinol (2013) 0.96
Adolescents with congenital adrenal hyperplasia because of 21-hydroxylase deficiency have vascular dysfunction. Clin Endocrinol (Oxf) (2012) 0.85
Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis. Indian J Endocrinol Metab (2013) 0.84
Enhanced magnetic field sensitivity of spin-dependent transport in cluster-assembled metallic nanostructures. Nat Mater (2006) 2.29
Ganglioneuroma of adrenal gland in a patient with Turner syndrome. Ann Diagn Pathol (2009) 1.06
[Complications of Meckel's diverticulum. Report of 42 cases]. Tunis Med (2009) 1.02
Probing one antiferromagnetic antiphase boundary and single magnetite domain using nanogap contacts. Nano Lett (2010) 0.94
A comparative study of the oxidative profile in Graves' disease, Hashimoto's thyroiditis, and papillary thyroid cancer. Biol Trace Elem Res (2010) 0.92
Long-term outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Am J Med Sci (2012) 0.91
48XXYY Syndrome in an Adult with Type 2 Diabetes Mellitus, Unilateral Renal Aplasia, and Pigmentary Retinitis. Case Rep Med (2010) 0.90
Genetic investigation of FOXE1 polyalanine tract in thyroid diseases: new insight on the role of FOXE1 in thyroid carcinoma. Cancer Biomark (2011) 0.90
Relationship between genetic polymorphisms of angiotensin-converting enzyme and methylenetetrahydrofolate reductase as risk factors for type 2 diabetes in Tunisian patients. Clin Biochem (2009) 0.90
Myeloperoxidase-antineutrophil cytoplasmic antibody-positive crescentic glomerulonephritis associated with benzylthiouracil therapy: report of the first case. Nephrol Dial Transplant (2003) 0.88
Polycarbonate microchannel network with carpet of gold nanowires as SERS-active device. Lab Chip (2009) 0.88
Hypermethylation of tumor-related genes in Tunisian patients with gastric carcinoma: clinical and biological significance. J Surg Oncol (2011) 0.88
PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage study. J Clin Endocrinol Metab (2003) 0.86
Leydig Cell Tumor Associated with Testicular Adrenal Rest Tumors in a Patient with Congenital Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency. Case Rep Urol (2012) 0.86
Genotypic interactions of renin-angiotensin system genes with diabetes type 2 in a Tunisian population. Life Sci (2010) 0.85
Microalbuminuria: a useful marker of cardiovascular disease. Iran J Kidney Dis (2013) 0.85
The heteroplasmic m.14709T>C mutation in the tRNA(Glu) gene in two Tunisian families with mitochondrial diabetes. J Diabetes Complications (2010) 0.84
Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis. Indian J Endocrinol Metab (2013) 0.84
Bartter syndrome revealed at adult age by recurrent nephrolithiasis, associated with hypertension and metabolic syndrome. Tunis Med (2011) 0.84
Analysis of MHC genes in a Tunisian isolate with autoimmune thyroid diseases: implication of TNF -308 gene polymorphism. J Autoimmun (2004) 0.83
[Carcinoid tumors of the appendix. A report of 46 cases]. Tunis Med (2004) 0.82
Complicated urinary tract infections associated with diabetes mellitus: Pathogenesis, diagnosis and management. Indian J Endocrinol Metab (2013) 0.82
Association analysis of interleukin gene polymorphisms in autoimmune thyroid diseases in the Tunisian population. Eur Cytokine Netw (2007) 0.82
[Gastric sarcoma]. Presse Med (2007) 0.82
Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patients. Hum Immunol (2012) 0.82
A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions. Biochem Biophys Res Commun (2013) 0.81
[Kinetics, diagnostic and prognostic value of procalcitonin after cardiac surgery]. Ann Biol Clin (Paris) (2012) 0.81
The mitochondrial ND1 m.3337G>A mutation associated to multiple mitochondrial DNA deletions in a patient with Wolfram syndrome and cardiomyopathy. Biochem Biophys Res Commun (2011) 0.81
No major genes in autoimmune thyroid diseases: complex segregation and epidemiological studies in a large Tunisian pedigree. J Genet (2011) 0.79
A potential role of TNFR gene polymorphisms in autoimmune thyroid diseases in the Tunisian population. Cytokine (2008) 0.79
Association between Leptin gene polymorphisms and plasma leptin level in three consanguineous families with obesity. Gene (2013) 0.79
Adrenal diseases during pregnancy: pathophysiology, diagnosis and management strategies. Am J Med Sci (2014) 0.78
Magnetization states of all-oxide spin valves controlled by charge-orbital ordering of coupled ferromagnets. Sci Rep (2013) 0.78
IL-1β a potential factor for discriminating between thyroid carcinoma and atrophic thyroiditis. Eur Cytokine Netw (2012) 0.78
[Breast cancer in men]. Presse Med (2007) 0.78
Thyroglobulin polymorphisms in Tunisian patients with autoimmune thyroid diseases (AITD). Immunobiology (2008) 0.78
A novel nonsense mutation in HSD17B3 gene in a Tunisian patient with sexual ambiguity. J Sex Med (2012) 0.77
Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency. Indian J Endocrinol Metab (2013) 0.77
SLC26A4 variations among Graves' hyper-functioning thyroid gland. Dis Markers (2010) 0.76
SLC26A4 expression among autoimmune thyroid tissues. Immunobiology (2010) 0.76
TNF gene polymorphisms in Graves' disease: TNF-308 A/G meta-analysis. Ann Hum Biol (2008) 0.76
Height outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Evidence from recent data. Indian J Endocrinol Metab (2013) 0.75
Adrenocortical Secreting Mass in a Patient with Gardner's Syndrome: A Case Report. Case Rep Med (2010) 0.75
Metabolic profile and cardiovascular risk factors in adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Indian J Endocrinol Metab (2012) 0.75
Isolated adrenocorticotropic hormone deficiency due to probable lymphocytic hypophysitis in a woman. Indian J Endocrinol Metab (2013) 0.75
Cerebral Aneurysms: A Rare Feature of Behçet's Disease-A Case Report and Review of the Literature. Case Rep Neurol Med (2013) 0.75
Oncocytome de la surrénale : Étude de cas. Can Urol Assoc J (2011) 0.75
Biexciton emission and crystalline quality of ZnO nano-objects. Nanotechnology (2011) 0.75
[Pancreatic endocrine tumor secreting growth hormone]. Ann Pathol (2005) 0.75
Absence of anti-pendrin auto-antibodies in the sera of Tunisian patients with autoimmune thyroid diseases. Clin Lab (2010) 0.75
[Pancreatic tuberculosis mimicking pancreatic neoplasia]. Tunis Med (2011) 0.75
Electrical-field-driven metal-insulator transition tuned with self-aligned atomic defects. Nanoscale (2015) 0.75
[Peritoneal gelatinous ascites]. Presse Med (2006) 0.75
Epidemiology of insulinoma in Tunisia. Endocrine (2011) 0.75
Cholestasis and protein-losing enteropathy secondary to hyperthyroidism in a 6-year-old girl. J Pediatr Endocrinol Metab (2014) 0.75
[Myeloid sarcoma of the main biliary duct]. Presse Med (2010) 0.75
A whole mitochondrial genome screening in a MELAS patient: a novel mitochondrial tRNA(Val) mutation. Biochem Biophys Res Commun (2011) 0.75
Evidence of association between FKBP1B and thyroid autoimmune disorders in a large Tunisian family. Autoimmunity (2004) 0.75
[Linitis plastica]. Presse Med (2007) 0.75
[Pancreas divisum]. Presse Med (2009) 0.75
Management of insulinoma: Tunisians' experience. Pancreas (2012) 0.75
[Heterotopic pregnancy]. Tunis Med (2008) 0.75
[Mechanisms of digoxin-induced gynecomastia: a case report and literature review]. Therapie (2012) 0.75
[Late post-operative adhesive small bowel occlusions. About 258 cases]. Tunis Med (2006) 0.75
[Solid pseudo papillary tumours of the pancreas]. Tunis Med (2008) 0.75
[Aspergillus flavus endocarditis of mechanical mitral valve]. Tunis Med (2008) 0.75
[Colorectal endocrine tumors]. Tunis Med (2011) 0.75
Synthesis of double mesoporous core-shell silica nanospheres with radially oriented mesopores via one-templating step using anionic surfactant. Chem Commun (Camb) (2010) 0.75
Ectopic secretion of GHRH by a pancreatic neuroendocrine tumor associated with an empty sella. Ann Endocrinol (Paris) (2011) 0.75
[Fibrocystic mastopathy and cancer of the breast. About 111 cases]. Tunis Med (2006) 0.75
[The results of laparoscopic treatment of the gallbladder lithiasis. About 500 cases]. Tunis Med (2007) 0.75
The Reliability and Concurrent Validity of a Modified Version of the International Physical Activity Questionnaire for Adolescents (IPAQ-A) in Tunisian Overweight and Obese Youths. Med Princ Pract (2015) 0.75
[Mucus secreting tumors of the appendix. Report of 22 cases]. Tunis Med (2004) 0.75
[A rare tumor of the main biliary duct]. Ann Pathol (2010) 0.75
[Systemic lupus erythematosus with autoimmune polyendocrinopathy type II]. Presse Med (2011) 0.75
[Inguinal hernia in a man with a uterus]. Tunis Med (2011) 0.75
Multifocal diabetic muscle infarction: a rare complication of poorly controlled diabetes mellitus. Intern Med (2014) 0.75
Association of intronic repetition of SLC26A4 gene with Hashimoto thyroiditis disease. Genet Res (Camb) (2013) 0.75
[Endoscopic thoracic sympatecomy for hyperhidrosis]. Tunis Med (2007) 0.75