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In‐vivo evaluations of bone regenerative potential of two novel bioactive glasses

Journal of biomedical materials research. Part A, 2023-08, Vol.111 (8), p.1264-1278

2023

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Recurrence of Hyperprolactinemia after Withdrawal of Long-Term Cabergoline Therapy

The journal of clinical endocrinology and metabolism, 2009-07, Vol.94 (7), p.2428-2436

2009

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Long-acting pasireotide improves clinical signs and quality of life in Cushing’s disease: results from a phase III study

Journal of endocrinological investigation, 2020-11, Vol.43 (11), p.1613-1622

2020

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The prognostic impact of the extent of ulceration in patients with clinical stage I–II melanoma: a multicentre study of the Italian Melanoma Intergroup (IMI)

British journal of dermatology (1951), 2021-02, Vol.184 (2), p.281-288

2021

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Acromegaly in the setting of Tatton-Brown-Rahman Syndrome

Pituitary, 2020-04, Vol.23 (2), p.167-170

2020

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The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes

Clinical genetics, 2010-11, Vol.78 (5), p.457-463

2010

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Associated changes in physiological parameters and spectral reflectance indices in olive (Olea europaea L.) leaves in response to different levels of water stress

International journal of remote sensing, 2008-03, Vol.29 (6), p.1725-1743

2008

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Early detection of biochemically occult autonomous thyroid nodules

European journal of endocrinology, 2016-12, Vol.175 (6), p.615

2016

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Deferred Radiation Therapy After Debulking of Nonfunctioning Pituitary Macroadenomas: An Appropriate Option

International journal of radiation oncology, biology, physics, 2016-10, Vol.96 (2), p.E77-E78

2016

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Immunological and microbiological periodontal profiles in isolated growth hormone deficiency

Journal of periodontology (1970), 2018-11, Vol.89 (11), p.1351-1361

2018

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Temozolomide retreatment in a recurrent prolactin-secreting pituitary adenoma: Hormonal and radiographic response

Journal of oncology pharmacy practice, 2016-06, Vol.22 (3), p.517-522

2016

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Usefulness of an ad hoc questionnaire (Acro-CQ) for the systematic assessment of acromegaly comorbidities at diagnosis and their management at follow-up

Journal of endocrinological investigation, 2016-11, Vol.39 (11), p.1277-1284

2016

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Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene

The journal of clinical endocrinology and metabolism, 1999-03, Vol.84 (3), p.917-923

1999

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Endocrinology and Art. Dwarf entertainers in the Roman Empire

Journal of endocrinological investigation, 2011-04, Vol.34 (4), p.333-333

2011

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Adrenal insufficiency

JAMA : the journal of the American Medical Association, 2005-11, Vol.294 (19), p.2481

Salvatori, Roberto

2005

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Pasiréotide LP mensuel diminue le cortisol libre urinaire et apporte un bénéfice clinique chez les patients avec maladie de Cushing : résultats à 12 mois de l’étude de phase III multicentrique, randomisée

Annales d'endocrinologie, 2016-09, Vol.77 (4), p.253-254

2016

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Decreased expression of the GHRH receptor gene due to a mutation in a Pit-1 binding site

Molecular endocrinology (Baltimore, Md.), 2002-03, Vol.16 (3), p.450-458

2002

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Cushing syndrome: maybe not so uncommon of an endocrine disease

Journal of the American Board of Family Medicine, 2012-03, Vol.25 (2), p.199

2012

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Treating Hypopituitarism in the Over 65s: Review of Clinical Studies

Clinical interventions in aging, 2023-01, Vol.18, p.423-439

2023

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A Mouse with Targeted Ablation of the Growth Hormone-Releasing Hormone Gene: A New Model of Isolated Growth Hormone Deficiency

Endocrinology (Philadelphia), 2004-09, Vol.145 (9), p.4134-4143

2004

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Effects of depot growth hormone replacement on thyroid function and volume in adults with congenital isolated growth hormone deficiency

Journal of endocrinological investigation, 2012-03, Vol.35 (3), p.265-268

2012

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Pasireotide Versus Octreotide in Acromegaly: A Head-to-Head Superiority Study

The journal of clinical endocrinology and metabolism, 2014-03, Vol.99 (3), p.791-799

2014

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An Intronic mutation is associated with prolactinoma in a young boy, decreased penetrance in his large family, and variable effects on MEN1 mRNA and protein

Hormone and metabolic research, 2009-08, Vol.41 (8), p.630

2009

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In-vivo short- and long-term evaluation of the interaction material-blood

Journal of materials science. Materials in medicine, 2005-12, Vol.16 (12), p.1213-1219

2005

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Thyrotoxicosis due to metastatic papillary thyroid cancer in a patient with Graves' disease

Journal of endocrinological investigation, 2002-07, Vol.25 (7), p.639-642

2002

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In‐vivo evaluations of bone regenerative potential of two novel bioactive glasses

Recurrence of Hyperprolactinemia after Withdrawal of Long-Term Cabergoline Therapy

Long-acting pasireotide improves clinical signs and quality of life in Cushing’s disease: results from a phase III study

The prognostic impact of the extent of ulceration in patients with clinical stage I–II melanoma: a multicentre study of the Italian Melanoma Intergroup (IMI)

Acromegaly in the setting of Tatton-Brown-Rahman Syndrome

The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes

Associated changes in physiological parameters and spectral reflectance indices in olive (Olea europaea L.) leaves in response to different levels of water stress

Early detection of biochemically occult autonomous thyroid nodules

Deferred Radiation Therapy After Debulking of Nonfunctioning Pituitary Macroadenomas: An Appropriate Option

Immunological and microbiological periodontal profiles in isolated growth hormone deficiency

Temozolomide retreatment in a recurrent prolactin-secreting pituitary adenoma: Hormonal and radiographic response

Usefulness of an ad hoc questionnaire (Acro-CQ) for the systematic assessment of acromegaly comorbidities at diagnosis and their management at follow-up

Familial dwarfism due to a novel mutation of the growth hormone-releasing hormone receptor gene

Endocrinology and Art. Dwarf entertainers in the Roman Empire

Adrenal insufficiency

Pasiréotide LP mensuel diminue le cortisol libre urinaire et apporte un bénéfice clinique chez les patients avec maladie de Cushing : résultats à 12 mois de l’étude de phase III multicentrique, randomisée

Decreased expression of the GHRH receptor gene due to a mutation in a Pit-1 binding site

Cushing syndrome: maybe not so uncommon of an endocrine disease

Treating Hypopituitarism in the Over 65s: Review of Clinical Studies

A Mouse with Targeted Ablation of the Growth Hormone-Releasing Hormone Gene: A New Model of Isolated Growth Hormone Deficiency

Effects of depot growth hormone replacement on thyroid function and volume in adults with congenital isolated growth hormone deficiency

Pasireotide Versus Octreotide in Acromegaly: A Head-to-Head Superiority Study

An Intronic mutation is associated with prolactinoma in a young boy, decreased penetrance in his large family, and variable effects on MEN1 mRNA and protein

In-vivo short- and long-term evaluation of the interaction material-blood

Thyrotoxicosis due to metastatic papillary thyroid cancer in a patient with Graves' disease

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