485 results on '"Shah, Nalini S"'
Search Results
2. Pituitary apoplexy in cushing’s disease: a single center study and systematic literature review
3. Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement
4. Inherited Fanconi renotubular syndromes: unveiling the intricacies of hypophosphatemic rickets/osteomalacia
5. Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic Review
6. Reversal of Basal Ganglia Hypermetabolism Following Surgical Removal of Adrenocorticotropic Hormone–Producing Lung Carcinoid in a Patient of Cushing Syndrome With Unusual Presentation of Acute Psychosis: Proof of Concept
7. POU1F1 mutations in combined pituitary hormone deficiency: differing spectrum of mutations in a Western-Indian cohort and systematic analysis of world literature
8. Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement
9. Genetic spectrum and predictors of mutations in four known genes in Asian Indian patients with growth hormone deficiency and orthotopic posterior pituitary: an emphasis on regional genetic diversity
10. Sympathetic Paraganglioma: A Single-Center Experience from Western India
11. Genotype phenotype correlation in Asian Indian von Hippel–Lindau (VHL) syndrome patients with pheochromocytoma/paraganglioma
12. High-Precision Conformal Fractionated Radiotherapy Is Effective In Achieving Remission In Patients With Acromegaly After Failed Transsphenoidal Surgery
13. Childhood Onset of Sulfonylurea Responsive Neonatal Diabetes Due to a Novel Homozygous Autosomal Recessive Mutation in the ABCC8 Gene which was Presumed to be Type 1B Diabetes Before Genetic Analysis
14. Paratesticular Paraganglioma
15. Glucocorticoid therapy as first-line treatment in primary hypophysitis: a systematic review and individual patient data meta-analysis
16. HRPT2- (CDC73) Related Hereditary Hyperparathyroidism: A Case Series From Western India
17. Ovotesticular Disorder of Sex Development: A Single-Center Experience
18. Primary Adrenal Lymphoma: a Single-Center Experience
19. Pituitary Gigantism - Experience of a Single Center from Western India
20. The Performance and Reproducibility of Late-Night Salivary Cortisol Estimation by Enzyme Immunoassay for Screening Cushing Disease
21. Disorders of the Adrenal Gland
22. Triple-A Syndrome
23. Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study
24. Multiple endocrine neoplasia type 1 syndrome: single centre experience from western India
25. Comparison of the Sensitivity of 68Ga-DOTATATE PET/CT with Other Imaging Modalities in Detecting Head and Neck Paraganglioma: Experience from Western India
26. Ectopic Acth-Secreting Syndrome: A Single-Center Experience
27. An Objective Olfactory Evaluation and its Correlation with Magnetic Resonance Imaging Findings in Asian Indian Patients with Idiopathic Hypogonadotropic Hypogonadism
28. Percentage arterial enhancement: An objective index for accurate identification of parathyroid adenoma/hyperplasia in primary hyperparathyroidism
29. Mucocolpos In A Toddler: Central Precocious Puberty With Vaginal Atresia
30. Performance of Plasma Fractionated Free Metanephrines by Enzyme Immunoassay In the Diagnosis Of Pheochromocytoma and Paraganglioma in Children
31. Primary (autoimmune) hypophysitis: a single centre experience
32. Peak Bone Mineral Density and Its Determinants in an Asian Indian Population
33. Luteinizing hormone β‐subunit deficiency: Report of a novel LHB likely pathogenic variant and a systematic review of the published literature
34. Genetically Confirmed Neonatal Diabetes: A Single Centre Experience
35. Performance of Plasma Fractionated free Metanephrines by Enzyme Immunoassay in the Diagnosis of Pheochromocytoma and Paraganglioma
36. Cushing Disease in Children and Adolescents: Twenty Years’ Experience in A Tertiary Care Center in India
37. Tumor-induced osteomalacia: a single center experience
38. 17β hydroxysteroid dehydrogenase 3 deficiency in 46,XY disorders of sex developmen t: our experience and a gender role‐focused systematic review
39. Clinical Spectrum of Adrenal Cushing’s Syndrome and the Caution for Interpretation of Adrenocorticotrophic Hormone: A Single-Center Experience
40. Raynaud's Phenomenon: Revisiting a Rare Sign of Pheochromocytoma and Paraganglioma
41. Encouraging efficacy of modern conformal fractionated radiotherapy in patients with uncured Cushing’s disease
42. Luteinizing hormone β‐subunit deficiency: Report of a novel LHB likely pathogenic variant and a systematic review of the published literature.
43. Efficacy of Cabergoline in Uncured (Persistent Or Recurrent) Cushing Disease after Pituitary Surgical Treatment with Or Without Radiotherapy
44. Treatment of Hypogonadism with Testosterone in Patients with Type 2 Diabetes Mellitus
45. Pilot Study to Evaluate the Effect of Short-Term Improvement in Vitamin D Status on Glucose Tolerance in Patients With Type 2 Diabetes Mellitus
46. Pheochromocytoma And Pregnancy:A Rare But Dangerous Combination
47. Prevalence and pattern of diabetic dyslipidemia in Indian type 2 diabetic patients
48. Giant Prolactinoma and Effectiveness of Medical Management
49. 17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature
50. Exonic WT1 pathogenic variants in 46,XY DSD associated with gonadoblastoma
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