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Keyword [Adrenal hyperplasia]
Result: 41 - 60 | Page: 3 of 4
41. A New Causative Gene ARMC5 Mutation Indentified By Whole-exome Sequencing In Primary Bilateral Macronodular Adrenal Hyperplasia
42. Clinical Characteristics Analysis Of 65 Patients With 21-hydroxylase Deficiency In Different ACTH Levels
43. Real-Time PCR-based Newborn Screening Of Severe Combined Immunodeficiency And Congenital Adrenal Hyperplasia
44. Clinical Case Analysis Of Congenital Adrenal Hyperplasia
45. Molecular Genetic Study Of The Family Of Patients With Congenital Adrenal Hyperplasia
46. Surgical Treatment Of Resistant Hypertension Combined With Primary Hyperaldosteronism Due To Adrenal Hyperplasia
47. The Pathogenesis Of ARMC5 Mutation Involved In Primary Bilateral Macronodular Adrenal Hyperplasia
48. NR0B1 Gene Mutation In A Case With X-linked Adrenal Hypoplasia Congenital
49. Clinical Study Of Rare Types Of ACTH-Independent Cushing's Syndrome
50. Comparison Of Clinical Characteristics Of Different Types Of Cushing's Syndrome And Analysis Of Influencing Factors Of Cardiovascular And Cerebrovascular Diseases
51. Clinical Data And Genetic Analysis Of 56 Cases Of Congenital Adrenal Hyperplasia
52. Study On Common TCM Syndromes Of Hypertension With Adrenal Hyperplasia
53. Progress Of Treatment For 21-hydroxylase Deficiency
54. Study On The Level Of Cortisol Hormone After Unilateral Laparoscopic Adrenalectomy
55. Clinical Analysis Of 8 Patients Of Congenital Lipoid Adrenal Hyperplasia
56. Theoretical Investigations On The Effects Of Mutations In Important Residues Of Cytochrome P45021A2 On Its Activity Using Molecular Dynamics Simulation
57. Correlation Between Genotype And Phenotype Of 21-hydroxylase Deficiency
58. A Case Report And Literature Review Of Familial Primary Bilateral Macronodular Adrenal Hyperplasia
59. Primary Bilateral Macronodular Adrenal Hyperlasia With ARMC5 Mutation:a Case Report And Literature Review
60. Prenatal Dexamethasone Treatment For Congenital Adrenal Hyperplasia
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