Professor of Medicine, Professor of Neurological Surgery, Johns Hopkins University School of Medicine; Medical Director, Johns Hopkins Pituitary Center
Endocrinology
Dr. Roberto Salvatori, MD
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Roberto Salvatori practices Endocrinology. He has 3 awards "CMS Meaningful Use Stage 1 Certification", "Top Doctors:Baltimore Area" and "Top Doctors:Washington-Baltimore". Roberto Salvatori, MD is a published MD. He published 90 publications, including: 'Growth Hormone Therapy Accelerates Axonal Regeneration, Promotes Motor Reinnervation, and Reduces Muscle Atrophy Following Peripheral Nerve Injury.' Roberto Salvatori is registered with Medicare and accepts Medicare payments.
Publications
- Growth Hormone Therapy Accelerates Axonal Regeneration, Promotes Motor Reinnervation, and Reduces Muscle Atrophy Following Peripheral Nerve Injury.
- MANAGEMENT OF CATECHOLAMINE-SECRETING TumorS IN PREGNANCY: A REVIEW.
- Letter to the Editor: Comment on "Effect of Growth Hormone Treatment on Fractures and Quality of Life in Postmenopausal Osteoporosis: A 10-Year Follow-Up Study" by Kra...
- Older individuals heterozygous for a Growth hormone-releasing hormone receptor gene mutation are shorter than normal subjects.
- Expression of the Pituitary stem/progenitor marker GFRα2 in human Pituitary adenomas and normal Pituitary.
- Liver status in congenital, untreated, isolated GH Deficiency.
- Perioperative Corticosteroid Management for Patients with Inflammatory Bowel Disease.
- Treatment of Hypopituitarism in patients receiving antiepileptic drugs.
- Surgical treatment of microprolactinomas: pros.
- Bladder pheochromocytoma.
- Perioperative Glucocorticoid Prescribing Habits in Patients With Inflammatory Bowel Disease : A Call for Standardization.
- Growth hormone should be used only for approved indications.
- Invasive adenoma and Pituitary carcinoma: a SEER database analysis.
- Isolated GH Deficiency due to a GHRH Receptor Mutation Causes Hip Joint Problems and Genu Valgum, and Reduces Size but not Density of Trabecular and Mixed Bone.
- Second attempt to withdraw cabergoline in prolactinomas: a pilot study.
- Lanreotide extended-release aqueous-gel formulation, injected by patient, partner or healthcare provider in patients with Acromegaly in the United States: 1-year data ...
- Management options for persistent postoperative Acromegaly.
- Expanded endonasal endoscopic approach for resection of a Growth hormone-secreting pituitary macroadenoma coexistent with a cavernous carotid artery aneurysm.
- "Glandular intoxication" following emergent tracheotomy during transsphenoidal surgery for Acromegaly: Cushing's 1910 unrecognized case of thyroid storm?
- ACTH-secreting pituitary microadenomas are associated with a higher prevalence of central hypothyroidism compared to other microadenoma Types.
- Pituitary Antibodies in Women with Hashimoto Thyroiditis: Prevalence in Diagnostic and Prediagnostic Sera.
- Recurrence of hyperprolactinemia after withdrawal of long-term cabergoline therapy.
- Synchronous GH- and prolactin-secreting Pituitary adenomas.
- Cystic bone lesion in the fifth metatarsal with subcutaneous rheumatoid nodule.
- GH, but not GHRH, plays a role in the development of experimental autoimmune encephalomyelitis.
- A Novel Frame Shift Mutation in the GHRH Receptor Gene in Familial Isolated GH Deficiency: Early Occurrence of Anterior Pituitary Hypoplasia.
- Nelfinavir induces radiation sensitization in Pituitary adenoma cells.
- Periodontal disease in adults with untreated congenital Growth hormone deficiency: a case-control study.
- Familial isolated Pituitary adenomas: from genetics to therapy.
- Cephalometric features in isolated Growth hormone deficiency.
- Effects of GH Deficiency and GH replacement on inter-male aggressiveness in mice.
- Effect of dopaminergic drug treatment on surgical findings in prolactinomas.
- Treatment of pituitary adenomas using radiosurgery and radiOtherapy: a single center experience and review of literature.
- On the shoulders of giants: Harvey Cushing's experience with Acromegaly and gigantism at the Johns Hopkins Hospital, 1896-1912.
- Clinical characteristics and therapeutic responses in patients with germ-line AIP mutations and Pituitary adenomas: an international collaborative study.
- Pituitary stem cells: review of the literature and current understanding.
- Complications and death among elderly patients undergoing Pituitary tumour surgery.
- Diseases associated with Growth hormone-releasing hormone receptor (GHRHR) mutations.
- Metabolic regulation of ghrelin O-acyl transferase (GOAT) expression in the mouse hypothalamus, Pituitary, and stomach.
- Adipokine profile and urinary albumin excretion in isolated Growth hormone deficiency.
- Longevity in untreated congenital Growth hormone deficiency due to a homozygous mutation in the GHRH receptor gene.
- Variations in referral patterns for hypophysectomies among pediatric patients with sellar and parasellar Tumors.
- Effectiveness of self- or partner-administration of an extended-release aqueous-gel formulation of lanreotide in lanreotide-naïve patients with Acromegaly.
- Clinical management of Growth hormone therapy in adults.
- Prognostic value of exercise echocardiography in diabetic patients.
- Pituitary and systemic autoimmunity in a case of intrasellar germinoma.
- Predictors of access to pituitary Tumor resection in the United States, 1988-2005.
- Mutation analysis of the muscarinic cholinergic receptor genes in isolated growth hormone deficiency Type IB.
- Partial rescue of Growth failure in Growth hormone (GH)-deficient mice by a single injection of a double-stranded adeno-associated viral vector expressing the GH gene ...
- Ectopic Cushing''s Syndrome: some facts.
- Quality of life in congenital, untreated, lifetime isolated Growth hormone deficiency.
- Effects of an oral Growth hormone secretagogue in older adults.
- Laryngeal and vocal evaluation in untreated Growth hormone deficient adults.
- Effect of dietary supplements of mussel and polychaetes on spawning performance of captive sole, Solea solea (Linnaeus, 1758).
- Adult-onset Growth hormone deficiency: causes, complications and treatment options.
- Consequences of lifetime isolated Growth hormone (GH) deficiency and effects of short-term GH treatment on bone in adults with a mutation in the GHRH-receptor gene.
- Climacteric in untreated isolated Growth hormone deficiency.
- A single injection of double-stranded adeno-associated viral vector expressing GH normalizes Growth in GH-deficient mice.
- Sizes of abdominal organs in adults with severe short stature due to severe, untreated, congenital GH Deficiency caused by a homozygous mutation in the GHRH receptor g...
- Congenital Growth hormone (GH) deficiency and atherosclerosis: effects of GH replacement in GH-naive adults.
- Vitamin A deficiency does not influence longitudinal Growth in mice.
- Metabolic effects of Growth hormone (GH) replacement in children and adolescents with severe isolated GH deficiency due to a GHRH receptor mutation.
- Heterozygosity for a mutation in the Growth hormone-releasing hormone receptor gene does not influence adult stature, but affects body composition.
- Cushing's Syndrome attributable to ectopic secretion of corticotropin in a patient with two neuroendocrine tumors.
- Once-daily administration of CJC-1295, a long-acting Growth hormone-releasing hormone (GHRH) analog, normalizes Growth in the GHRH knockout mouse.
- Effects of combined long-term treatment with a Growth hormone-releasing hormone analogue and a Growth hormone secretagogue in the Growth hormone-releasing hormone knoc...
- Lack of evidence of premature atherosclerosis in untreated severe isolated Growth hormone (GH) deficiency due to a GH-releasing hormone receptor mutation.
- Autosomal-dominant isolated growth hormone deficiency (IGHD Type II) with normal GH-1 gene.
- Thyroid morphology and function in adults with untreated isolated Growth hormone deficiency.
- Influence of estrogen administration on the Growth response to Growth hormone (GH) in GH-deficient mice.
- Naturally-occurring missense mutations in the human Growth hormone-releasing hormone receptor alter ligand binding.
- Effects of long-term treatment with Growth hormone-releasing peptide-2 in the GHRH knockout mouse.
- Effects of recombinant mouse Growth hormone treatment on Growth and body composition in GHRH knock out mice.
- Giant somatotrophinoma without acromegalic features: more "quiet" than "silent": case report.
- [Growth or somatotrophic hormone: new perspectives in isolated GH deficiency after description of the mutation in the GHRH receptor gene in individuals of Itabaianinha...
- Partial reversibility of Growth hormone (GH) deficiency in the GH-releasing hormone (GHRH) knockout mouse by postnatal treatment with a GHRH analog.
- Mpl Baltimore: a thrombopoietin receptor polymorphism associated with thrombocytosis.
- Impact of fluconazole prophylaxis on cortisol levels in critically ill surgical patients.
- Familial Growth Hormone Deficiency and Mutations in the GHRH Receptor Gene.
- A mouse with targeted ablation of the Growth hormone-releasing hormone gene: a new model of isolated Growth hormone deficiency.
- Variability in anterior pituitary size within members of a family with GH Deficiency due to a new splice mutation in the GHRH receptor gene.
- Images in clinical medicine. Pemberton's sign.
- Growth hormone and IGF-1.
- Magnetic resonance imaging study of Pituitary morphology in subjects homozygous and heterozygous for a null mutation of the GHRH receptor gene.
- A new missense mutation in the Growth hormone-releasing hormone receptor gene in familial isolated GH deficiency.
- Serum GH response to pharmacological stimuli and physical exercise in two siblings with two new inactivating mutations in the GH-releasing Hormone receptor gene.
- Detection of a recurring mutation in the human Growth hormone-releasing hormone receptor gene.
- Familial isolated Growth hormone deficiency is associated with increased systolic blood pressure, central obesity, and dyslipidemia.
- Decreased expression of the GHRH receptor gene due to a mutation in a Pit-1 binding site.
Schools
University of Rome Tor Vergata Faculty of Medicine And Surgery
Montefiore Mc
Johns Hopkins Hospital
Ny Hospital Cornell University
Conditions Treated
- Acromegaly and Gigantism
- Adrenal Incidentaloma
- Adrenal Insufficiency
- Craniopharyngioma
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Doctors Specialties
- Endocrinology
Accepted Insurances
Awards
- CMS Meaningful Use Stage 1 Certification
- Top Doctors:Baltimore Area
- Top Doctors:Washington-Baltimore
Education
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Johns Hopkins University -
New York Presbyterian Hospital - Cornell Campus -
University of Cattolica del Sacro Cuore
Hospital
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Johns Hopkins Hospital
Drug Facts
| NPI NUMBER | 1063444529 | |
| NPPES Provider LastName | SALVATORI | |
| NPPES Provider FirstName | ROBERTO | |
| NPPES Provider ZIPCode | 212870005 | |
| NPPES Provider State | MD | |
| Specialty Description | Internal Medicine | |
| Total Claim Count | 358.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1063444529 |
| Last Name Of The Provider | SALVATORI |
| First Name Of The Provider | ROBERTO |
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