High prevalence of pituitary adenomas: A cross-sectional study in the province of Liège, J Clin Endocrinol Metab, vol.91, issue.12, pp.4769-4775, 2006. ,
Incidental pituitary lesions in 1,000 unselected autopsy specimens, Radiology, vol.193, issue.1, pp.161-164, 1994. ,
Carney complex: an update, Eur J Endocrinol, vol.173, issue.4, pp.85-97, 2015. ,
Acromegaly associated with phaeochromocytoma, Acta Med Scand, vol.142, issue.1, pp.1-5, 1952. ,
Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1), J Clin Endocrinol Metab, vol.97, issue.9, pp.2990-3011, 2012. ,
Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice, J Clin Endocrinol Metab, vol.100, issue.5, pp.710-719, 2015. ,
Pheochromocytomas and pituitary adenomas in three patients with MAX exon deletions, Endocrine-Related Cancer. England, vol.25, pp.37-42, 2018. ,
Case Report of a Prolactinoma in a Patient With a Novel MAX Mutation and Bilateral Pheochromocytomas, J Endocr Soc, vol.1, issue.11, pp.1401-1408, 2017. ,
The association of pituitary adenomas and phaeochromocytomas or paragangliomas, Endocr Relat Cancer, vol.22, issue.4, pp.105-127, 2015. ,
HGVS Recommendations for the Description of Sequence Variants, Update. Hum Mutat, vol.37, issue.6, pp.564-573, 2016. ,
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College 32 ,
, Genet Med, vol.17, issue.5, pp.405-424, 2015.
Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency, Hum Mol Genet, vol.13, issue.6, pp.659-67, 2004. ,
High prevalence of pituitary adenomas: A cross-sectional study in the province of Liège, J Clin Endocrinol Metab, vol.91, issue.12, pp.4769-75, 2006. ,
UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present, p.1676 ,
URL : https://hal.archives-ouvertes.fr/hal-01975538
, Patients from the French Population, J Clin Endocrinol Metab, 2018.
Acromegaly in Carney complex, Pituitary [Internet], 2019. ,
MEN4 and CDKN1B mutations: The latest of the MEN syndromes, Endocr Relat Cancer, vol.24, issue.10, pp.195-208, 2017. ,
Clinical Features of Multiple Endocrine Neoplasia Type 4: Novel Pathogenic Variant and Review of Published Cases, J Clin Endocrinol Metab ,
A new prognostic clinicopathological classification of pituitary adenomas: a multicentric case-control study of 410 patients with 8 years post-operative follow-up, Acta Neuropathol, vol.126, issue.1, pp.123-158, 2013. ,
URL : https://hal.archives-ouvertes.fr/hal-00875723
SDHA related tumorigenesis : a new case series and literature review for variant interpretation and pathogenicity, pp.237-50, 2017. ,
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SDHC mutation in an elderly patient without familial antecedents, Clin Endocrinol (Oxf), vol.69, issue.6, pp.906-916, 2008. ,
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, Succinate dehydrogenase (SDH) D subunit (SDHD) inactivation in a growth-Besides AIP don't forget MEN1 genetic analysis, Eur J Endocrinol, 2013.
Analysis of the MEN1 gene in sporadic pituitary adenomas, J Pathol, vol.188, issue.2, pp.168-73, 1999. ,
Mild pituitary phenotype in 3-and 12-month-old Aip-deficient male mice, J Endocrinol, vol.231, issue.1, pp.59-69, 2016. ,
Hyperplasia-adenoma sequence in pituitary tumorigenesis related to aryl hydrocarbon receptor interacting protein gene mutation, Endocr Relat Cancer, vol.18, issue.3, pp.347-56, 2011. ,
Pituitary Pathology in Carney Complex Patients, Pituitary, vol.7, issue.2, pp.73-82, 2004. ,
Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation, N Engl J Med, vol.371, issue.25, pp.2363-74, 2014. ,
The 3PAs: An Update on the Association of Pheochromocytomas, Paragangliomas, and Pituitary Tumors, Horm Metab Res, vol.51, issue.07, pp.419-455, 2019. ,
SDH mutations in cancer, Biochim Biophys Acta -Bioenerg, vol.1807, issue.11, pp.1432-1475, 2011. ,
Succinate dehydrogenase (SDHx) mutations in pituitary tumors: could this be a new role for mitochondrial complex II and/or Krebs cycle defects? Endocr Relat Cancer, vol.19, pp.33-40, 2012. ,
Fatal hypothermia related vacuolation of hormone-producing cells in the anterior pituitary, Leg Med, vol.6, issue.3, pp.157-63, 2004. ,
Microscopic examination of pituitary glands in cases of fatal accidental hypothermia, Forensic Sci Res, vol.2, issue.3, pp.132-140, 2017. ,
, Interactions and Molecular Regulatory Mechanisms, vol.35, pp.615-636, 2015.
Succinate dehydrogenase (SDH)-deficient neoplasia, Histopathology, vol.72, issue.1, pp.106-122, 2018. ,
Clinical aspects of SDHArelated pheochromocytoma and paraganglioma: A nationwide study, J Clin Endocrinol Metab, vol.103, issue.2, pp.438-445, 2018. ,
Bayesian approach to determining penetrance of pathogenic SDH variants, J Med Genet, vol.55, issue.11, pp.729-763, 2018. ,
Pathogenicity and Penetrance of Germline SDHA Variants in Pheochromocytoma and Paraganglioma ( PPGL ), vol.2, pp.806-822, 2018. ,
The role of complex II in disease, Biochim Biophys Acta Bioenerg [Internet], vol.1827, issue.5, pp.543-51, 2013. ,
Pheochromocytoma and paraganglioma: An endocrine society clinical practice guideline, J Clin Endocrinol Metab, vol.99, issue.6, pp.1915-1919, 2014. ,
High prevalence of pituitary adenomas: A cross-sectional study in the province of Liège, J Clin Endocrinol Metab, vol.91, issue.12, pp.4769-4775, 2006. ,
Incidental pituitary lesions in 1,000 unselected autopsy specimens, Radiology, vol.193, issue.1, pp.161-164, 1994. ,
Carney complex: an update, Eur J Endocrinol, vol.173, issue.4, pp.85-97, 2015. ,
Acromegaly associated with phaeochromocytoma, Acta Med Scand, vol.142, issue.1, pp.1-5, 1952. ,
Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1), J Clin Endocrinol Metab, vol.97, issue.9, pp.2990-3011, 2012. ,
Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice, J Clin Endocrinol Metab, vol.100, issue.5, pp.710-719, 2015. ,
Pheochromocytomas and pituitary adenomas in three patients with MAX exon deletions, Endocrine-Related Cancer. England, vol.25, pp.37-42, 2018. ,
Case Report of a Prolactinoma in a Patient With a Novel MAX Mutation and Bilateral Pheochromocytomas, J Endocr Soc, vol.1, issue.11, pp.1401-1408, 2017. ,
The association of pituitary adenomas and phaeochromocytomas or paragangliomas, Endocr Relat Cancer, vol.22, issue.4, pp.105-127, 2015. ,
HGVS Recommendations for the Description of Sequence Variants, Update. Hum Mutat, vol.37, issue.6, pp.564-573, 2016. ,
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College 63 ,
, Genet Med, vol.17, issue.5, pp.405-424, 2015.
Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency, Hum Mol Genet, vol.13, issue.6, pp.659-67, 2004. ,
High prevalence of pituitary adenomas: A cross-sectional study in the province of Liège, J Clin Endocrinol Metab, vol.91, issue.12, pp.4769-75, 2006. ,
UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present, p.1676 ,
URL : https://hal.archives-ouvertes.fr/hal-01975538
, Patients from the French Population, J Clin Endocrinol Metab, 2018.
Acromegaly in Carney complex, Pituitary [Internet], 2019. ,
MEN4 and CDKN1B mutations: The latest of the MEN syndromes, Endocr Relat Cancer, vol.24, issue.10, pp.195-208, 2017. ,
Clinical Features of Multiple Endocrine Neoplasia Type 4: Novel Pathogenic Variant and Review of Published Cases, J Clin Endocrinol Metab ,
A new prognostic clinicopathological classification of pituitary adenomas: a multicentric case-control study of 410 patients with 8 years post-operative follow-up, Acta Neuropathol, vol.126, issue.1, pp.123-158, 2013. ,
URL : https://hal.archives-ouvertes.fr/hal-00875723
SDHA related tumorigenesis : a new case series and literature review for variant interpretation and pathogenicity, pp.237-50, 2017. ,
,
SDHC mutation in an elderly patient without familial antecedents, Clin Endocrinol (Oxf), vol.69, issue.6, pp.906-916, 2008. ,
,
, Succinate dehydrogenase (SDH) D subunit (SDHD) inactivation in a growth
Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes, J Clin Endocrinol Metab, vol.91, issue.3, pp.827-863, 2006. ,
Novel genetic causes of pituitary adenomas, Clin Cancer Res, vol.22, issue.20, pp.5030-5072, 2016. ,
Germline inactivating mutations of the aryl hydrocarbon receptor-interacting protein gene in a large cohort of sporadic acromegaly: Mutations are found in a subset of young patients with Macroadenomas, Eur J Endocrinol, vol.157, issue.1, pp.1-8, 2007. ,
Prevalence of AIP mutations in a large series of sporadic Italian acromegalic patients and evaluation of CDKN1B status in acromegalic patients with multiple endocrine neoplasia, Eur J Endocrinol, vol.163, issue.3, pp.369-76, 2010. ,
Prevalence of AIP mutations in a series of Turkish acromegalic patients: are synonymous AIP mutations relevant? Pituitary, vol.18, pp.831-838, 2015. ,
Analysis of GPR101 and AIP genes mutations in acromegaly: a multicentric study, Endocrine, vol.54, issue.3, pp.762-769, 2016. ,
Frequency of AIP gene mutations in young patients with acromegaly: A registrybased study, J Clin Endocrinol Metab, vol.99, issue.12, pp.2789-93, 2014. ,
Landscape of familial isolated and young-onset pituitary adenomas: Prospective diagnosis in AIP mutation carriers, J Clin Endocrinol Metab, 2015. ,
High prevalence of AIP gene mutations following focused screening in young patients with sporadic pituitary Macroadenomas, Eur J Endocrinol, vol.165, issue.4, pp.509-524, 2011. ,
URL : https://hal.archives-ouvertes.fr/hal-00755667
Genetic analysis in young patients with sporadic pituitary Macroadenomas, p.66 ,
URL : https://hal.archives-ouvertes.fr/hal-00933803
, Besides AIP don't forget MEN1 genetic analysis, Eur J Endocrinol, 2013.
Analysis of the MEN1 gene in sporadic pituitary adenomas, J Pathol, vol.188, issue.2, pp.168-73, 1999. ,
Mild pituitary phenotype in 3-and 12-month-old Aip-deficient male mice, J Endocrinol, vol.231, issue.1, pp.59-69, 2016. ,
Hyperplasia-adenoma sequence in pituitary tumorigenesis related to aryl hydrocarbon receptor interacting protein gene mutation, Endocr Relat Cancer, vol.18, issue.3, pp.347-56, 2011. ,
Pituitary Pathology in Carney Complex Patients, Pituitary, vol.7, issue.2, pp.73-82, 2004. ,
Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation, N Engl J Med, vol.371, issue.25, pp.2363-74, 2014. ,
The 3PAs: An Update on the Association of Pheochromocytomas, Paragangliomas, and Pituitary Tumors, Horm Metab Res, vol.51, issue.07, pp.419-455, 2019. ,
SDH mutations in cancer, Biochim Biophys Acta -Bioenerg, vol.1807, issue.11, pp.1432-1475, 2011. ,
Succinate dehydrogenase (SDHx) mutations in pituitary tumors: could this be a new role for mitochondrial complex II and/or Krebs cycle defects? Endocr Relat Cancer, vol.19, pp.33-40, 2012. ,
Fatal hypothermia related vacuolation of hormone-producing cells in the anterior pituitary, Leg Med, vol.6, issue.3, pp.157-63, 2004. ,
Microscopic examination of pituitary glands in cases of fatal accidental hypothermia, Forensic Sci Res, vol.2, issue.3, pp.132-140, 2017. ,
, Interactions and Molecular Regulatory Mechanisms, vol.35, pp.615-636, 2015.
Succinate dehydrogenase (SDH)-deficient neoplasia, Histopathology, vol.72, issue.1, pp.106-122, 2018. ,
Clinical aspects of SDHArelated pheochromocytoma and paraganglioma: A nationwide study, J Clin Endocrinol Metab, vol.103, issue.2, pp.438-445, 2018. ,
Bayesian approach to determining penetrance of pathogenic SDH variants, J Med Genet, vol.55, issue.11, pp.729-763, 2018. ,
Pathogenicity and Penetrance of Germline SDHA Variants in Pheochromocytoma and Paraganglioma ( PPGL ), vol.2, pp.806-822, 2018. ,
The role of complex II in disease, Biochim Biophys Acta Bioenerg [Internet], vol.1827, issue.5, pp.543-51, 2013. ,
Pheochromocytoma and paraganglioma: An endocrine society clinical practice guideline, J Clin Endocrinol Metab, vol.99, issue.6, pp.1915-1957, 2014. ,