F. Schillo
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View article: Hypoparathyroidism after total thyroidectomy: reactive to symptoms supplementation
Hypoparathyroidism after total thyroidectomy: reactive to symptoms supplementation Open
Supplementing only symptomatic patients was safe and efficient. This attitude does not alter on morbidity, mortality or readmission rate which is in line with current literature.
View article: Data from <i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma
Data from <i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma Open
Purpose: Pheochromocytomas (PCC) and paragangliomas (PGL) are genetically heterogeneous neural crest–derived neoplasms. Recently we identified germline mutations in a new tumor suppressor susceptibility gene, MAX (MYC-associated factor X),…
View article: Supplementary Figures 1 - 3 from <i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma
Supplementary Figures 1 - 3 from <i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma Open
PDF file, 794KB, Supplementary figure S1. Gross MAX deletion analysis Supplementary figure S2. Immunohistochemical assessment. Supplementary figure S3. Pedigree of 3 families with affected relatives in more than one generation.
View article: Supplementary Figures 1 - 3 from <i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma
Supplementary Figures 1 - 3 from <i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma Open
PDF file, 794KB, Supplementary figure S1. Gross MAX deletion analysis Supplementary figure S2. Immunohistochemical assessment. Supplementary figure S3. Pedigree of 3 families with affected relatives in more than one generation.
View article: Data from <i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma
Data from <i>MAX</i> Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma Open
Purpose: Pheochromocytomas (PCC) and paragangliomas (PGL) are genetically heterogeneous neural crest–derived neoplasms. Recently we identified germline mutations in a new tumor suppressor susceptibility gene, MAX (MYC-associated factor X),…
View article: Predictive Factors of Somatostatin Receptor Ligand Response in Acromegaly—A Prospective Study
Predictive Factors of Somatostatin Receptor Ligand Response in Acromegaly—A Prospective Study Open
Context Somatostatin receptor ligands (SRLs) are the cornerstone medical treatments for acromegaly; however, many patients remain unresponsive to SRLs. Well-established predictive markers of response are needed. Objective We aimed to explo…
View article: Aggressive pituitary tumours and carcinomas, characteristics and management of 171 patients
Aggressive pituitary tumours and carcinomas, characteristics and management of 171 patients Open
Objective To describe clinical and pathological characteristics and treatment outcomes in a large cohort of aggressive pituitary tumours (APT)/pituitary carcinomas (PC). Design Electronic survey August 2020–May 2021. Results 96% of 171 (12…
View article: T2-weighted MRI signal predicts hormone and tumor responses to somatostatin analogs in acromegaly
T2-weighted MRI signal predicts hormone and tumor responses to somatostatin analogs in acromegaly Open
GH-secreting pituitary adenomas can be hypo-, iso- or hyper-intense on T2-weighted MRI sequences. We conducted the current multicenter study in a large population of patients with acromegaly to analyze the relationship between T2-weighted …
View article: Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey
Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey Open
We report the spectrum of testicular/gonadotrope axis impairment in the largest cohort of 21OHD men studied to date. Our results suggest that French men with 21OHD managed in specialized centers frequently have impaired exocrine testicular…