Professor Jointly of The Department of Endocrine Neoplasia and Hormonal Disorders, Division of Internal Medicine and The Department of Pediatrics Patient Care, Division of Pediatrics at The University of Texas MD Anderson Cancer Center
Pediatric Endocrinology
Dr. Steven G. Waguespack, MD
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Steven Waguespack practices Pediatric Endocrinology. He attended Indiana University School of Medicine. Indiana University School of Medicine is ranked 45 in research and 47 in primary care medicine He over the years received 4 awards: "America's Top Doctors", "Top Doctors:SE Texas", "America's Top Doctors for Cancer" and "Fellow (FAAP)". Dr. Steven G. Waguespack is also a published physician. He has 73 publication published. The most recent publication is: Survey of antibiotic susceptibility among gram-negative bacilli at a cancer center. He accepts Medicare.
Publications
- Preexisting Adrenal masses in patients with adrenocortical carcinoma: clinical and radiological factors contributing to delayed diagnosis.
- Revised American Thyroid Association Guidelines for the Management of Medullary Thyroid Carcinoma The American Thyroid Association Guidelines Task Force on Medullary T...
- Efficacy and tolerability of vemurafenib in patients with BRAF(V600E) -positive papillary Thyroid cancer: M.D. Anderson Cancer Center off label experience.
- Fatal juvenile xanthogranuloma presenting as a sellar lesion: case report and literature review.
- Thyroid carcinoma, version 2.2014.
- BRAF inhibitor dabrafenib in patients with metastatic BRAF-mutant Thyroid cancer.
- Role of salvage targeted therapy in differentiated Thyroid cancer patients who failed first-line sorafenib.
- Preoperative multiple endocrine neoplasia type 1 diagnosis improves the surgical outcomes of pediatric patients with primary hyperparaThyroidism.
- Efficacy and Tolerability of Different Starting Doses of Sorafenib in Patients With Differentiated Thyroid Cancer.
- Prevalence by Age and Predictors of Medullary Thyroid Cancer in Patients with Lower Risk Germline RET Proto-Oncogene Mutations.
- A 67-Year-Old Man With a Midline Neck Mass.
- Feasibility and outcome of re-irradiation in the treatment of multiply recurrent pituitary adenomas.
- Adrenocortical carcinoma: Clinical outcomes and prognosis of 330 patients at a tertiary care center.
- The Characterization of Pheochromocytoma and Its Impact on Overall Survival in Multiple Endocrine Neoplasia Type 2.
- Adrenal Ganglioneuroma: Features and outcomes of 27 cases at a referral cancer center.
- Bone Metastases and Skeletal-Related Events in Patients With Malignant Pheochromocytoma and Sympathetic Paraganglioma.
- Long-term follow-up data may help manage patient and parent expectations for pediatric patients undergoing Thyroidectomy.
- The Noninvestigational Use of Tyrosine Kinase Inhibitors in Thyroid Cancer: Establishing a Standard for Patient Safety and Monitoring.
- A Retrospective Cohort Analysis of the Efficacy of Adjuvant Radiotherapy after Primary Surgical Resection in Patients With Adrenocortical Carcinoma.
- Treatment With Sunitinib for Patients With Progressive Metastatic Pheochromocytomas and Sympathetic Paragangliomas.
- Ultrasonography Should Not Guide the Timing of Thyroidectomy in Pediatric Patients Diagnosed with Multiple Endocrine Neoplasia Syndrome 2A through Genetic Screening.
- Long-term outcome of comprehensive central compartment dissection in patients with recurrent/persistent papillary Thyroid carcinoma.
- Phospho-histone H3 (pHH3) immuno-reactivity as a prognostic marker in non-functioning pituitary adenomas.
- Inhibition of the Ras/Raf/MEK/ERK and RET Kinase Pathways With the Combination of the Multikinase Inhibitor Sorafenib and the Farnesyltransferase Inhibitor Tipifarnib ...
- Random postoperative day 3 cortisol as a predictor of hypothalamic-pituitary-Adrenal axis integrity after transsphenoidal surgery.
- Acute-Onset Ectopic Adrenocorticotropic Hormone Syndrome Secondary to Metastatic Endometrioid Carcinoma of the Ovaries As a Fatal Complication.
- Cushing Syndrome secondary to ectopic adrenocorticotropic hormone secretion: the University of Texas MD Anderson Cancer Center Experience.
- Medical management of postsurgical hypoparaThyroidism.
- Multiple endocrine neoplasia type 2B with a RET proto-oncogene A883F mutation displays a more indolent form of medullary Thyroid carcinoma compared with a RET M918T mu...
- Do the recent American Thyroid Association (ATA) Guidelines accurately guide the timing of prophylactic Thyroidectomy in MEN2A?
- Initial management and follow-up of differentiated Thyroid cancer in children.
- Spontaneous involution of Rathke cleft cysts: is it rare or just underreported?
- Treatment with tyrosine kinase inhibitors for patients with differentiated Thyroid cancer: the M. D. Anderson experience.
- Multiple endocrine neoplasia [corrected] syndrome type 2B in early childhood: long-term benefit of prophylactic Thyroidectomy.
- Surgical management of nonMultiple endocrine neoplasia endocrinopathies: state-of-the-art review.
- Approach and safety of comprehensive central compartment dissection in patients with recurrent papillary Thyroid carcinoma.
- Thyroid cancer in young adults.
- A perspective from pediatric endocrinology on the hereditary medullary Thyroid carcinoma syndromes.
- The successful use of sorafenib to treat pediatric papillary Thyroid carcinoma.
- Use of the tyrosine kinase inhibitor sunitinib in a patient With von Hippel-Lindau disease: targeting angiogenic factors in pheochromocytoma and other von Hippel-Linda...
- Multisystem crisis in a patient With presumptive renal cell carcinoma.
- A novel von Hippel-Lindau point mutation presents as apparently sporadic pheochromocytoma.
- Recent advances in Thyroid cancer. In brief.
- Recent advances in Thyroid cancer.
- Failure to recognize Multiple endocrine neoplasia 2B: more common than we think?
- Primary Adrenal natural killer/T-cell nasal type lymphoma: first case report in adults.
- Transient hypophysitis after cytotoxic T lymphocyte-associated antigen 4 (CTLA4) blockade.
- Autosomal dominant osteopetrosis: clinical severity and natural history of 94 subjects With a chloride channel 7 gene mutation.
- Management of pancreatic endocrine tumors in multiple endocrine neoplasia Type 1.
- Analysis of variation in expression of autosomal dominant osteopetrosis Type 2: searching for modifier genes.
- Adrenal ganglioneuromas in children with multiple endocrine neoplasia type 2: a report of two cases.
- Image in endocrinology: Adrenal pseudocyst.
- Severe infantile hypercalcemia associated with Williams Syndrome successfully treated with intravenously administered pamidronate.
- ParaThyroid carcinoma: a 22-year experience.
- Osteoclast-derived serum tartrate-resistant acid phosphatase 5b in Albers-Schonberg disease (Type II autosomal dominant osteopetrosis).
- Surgical management of hereditary pheochromocytoma.
- Expansile intraosseus lesion of the mandible.
- Chloride channel 7 (ClCN7) gene mutations and autosomal dominant osteopetrosis, Type II.
- Acute painful neuropathy (insulin neuritis) in a boy following rapid glycemic control for type 1 Diabetes mellitus.
- Measurement of tartrate-resistant acid phosphatase and the brain isoenzyme of creatine kinase accurately diagnoses Type II autosomal dominant osteopetrosis but does no...
- Case 29-2001: oncogenic hypophosphatemic osteomalacia.
- Survey of antibiotic susceptibility among gram-negative bacilli at a cancer center.
- Metastatic melanoma to the pituitary gland.
- A current review of the etiology, diagnosis, and treatment of pediatric pheochromocytoma and paraganglioma.
- FGF-23 in fibrous dysplasia of bone and its relationship to Renal phosphate wasting.
- Thyroid carcinoma.
- A catecholamine crisis on Mount Kilimanjaro: a hypoxia effect?
- Medullary carcinoma.
- Clinical risk factors for malignancy and overall survival in patients With pheochromocytomas and sympathetic paragangliomas: primary tumor size and primary tumor locat...
- Pilot trial of sunitinib therapy in patients With von Hippel-Lindau disease.
- Management of medullary Thyroid carcinoma and MEN2 syndromes in childhood.
- Gonadotropin-dependent precocious puberty: neoplastic causes and Endocrine considerations.
Schools
U Of Tx Med Sch At Houston
Indiana University Med Center
Indiana University Med Center Riley Children39S Hospital
Conditions Treated
- Abnormal Thyroid
- Acromegaly and Gigantism
- AdRenal Incidentaloma
- AdRenal Insufficiency
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Doctors Specialties
- Pediatric Endocrinology
Accepted Insurances
Awards
- America's Top Doctors
- Top Doctors:SE Texas
- America's Top Doctors for Cancer
- Fellow (FAAP)
Education
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Indiana University School of Medicine -
University of Texas Medical School
Hospital
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University of Texas M.D. Anderson Cancer Center
Drug Facts
| NPI NUMBER | 1861593170 | |
| NPPES Provider LastName | WAGUESPACK | |
| NPPES Provider FirstName | STEVEN | |
| NPPES Provider ZIPCode | 770304009 | |
| NPPES Provider State | TX | |
| Specialty Description | Endocrinology | |
| Total Claim Count | 616.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1861593170 |
| Last Name Of The Provider | WAGUESPACK |
| First Name Of The Provider | STEVEN |
| View All |
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