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2. Diagnosis and management of prolactin-secreting pituitary adenomas: a Pituitary Society international Consensus Statement

3. Implementation of a Standardized Interdisciplinary Perioperative Protocol for Patients Undergoing Transsphenoidal Surgery: Impact on Patient Outcomes

4. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

5. The clinical presentation of PIT1 positive pituitary neuroendocrine tumor immunonegative for growth hormone, prolactin, and thyroid stimulating hormone with analysis of clinical and immunostaining dissociation

7. Author Correction: Diagnosis and management of prolactin-secreting pituitary adenomas: a Pituitary Society international Consensus Statement

12. Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

13. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

15. Managing high blood sugar (hyperglycemia) during pasireotide treatment:A plain language summary of the B2219 study

16. Oral octreotide capsules for acromegaly treatment: application of clinical trial insights to real-world use.

17. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling

21. Multidisciplinary management of acromegaly: A consensus

23. Predictive factors and the management of hyperglycemia in patients with acromegaly and Cushing's disease receiving pasireotide treatment: post hoc analyses from the SOM230B2219 study.

24. Biallelic CRELD1 variants cause a multisystem syndrome including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.

25. Author Correction: Diagnosis and management of prolactin-secreting pituitary adenomas: a Pituitary Society international Consensus Statement

26. Determining call-to-entry rate and recruitment barriers in clinical studies for community clinics serving low-income populations: a cohort study

27. Endocrine disorders

28. List of contributors

30. Silent Corticotroph Adenomas: An Aggressive Tumor Type That Merits Appropriate Preoperative Characterization.

31. Twenty-Four-Hour Discharge following Transsphenoidal Resection of Pituitary Adenomas: Safety and Feasibility of a Pituitary-Center Cohort.

32. Current Role of Endoscopic Endonasal Approach for Craniopharyngiomas: A 10-Year Systematic Review and Meta-Analysis Comparison with the Open Transcranial Approach

35. Atypical Alexander disease with dystonia, retinopathy, and a brain mass mimicking astrocytoma

41. Durable biochemical response and safety with oral octreotide capsules in acromegaly

43. American Association of Clinical Endocrinology Clinical Practice Guideline: Developing a Diabetes Mellitus Comprehensive Care Plan—2022 Update

46. Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

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