Back to Search
SHARON GOUGH, LPCC LADAC PH.D
LPCC LADAC PH.D
Professional Counselor
NPI: 1750554374Individual
Specialties, Licenses & Credentials
Addiction (Substance Use Disorder) Counselor
Counselor — Addiction (Substance Use Disorder)
Code: 101YA0400X
10681(TX)
Professional CounselorPrimary
Counselor — Professional
Code: 101YP2500X
63100(TX)
Research & Publications (20)
Quinolines as a novel structural class of potent and selective PDE4 inhibitors. Optimisation for inhaled administration.
PMID 19656678·Bioorg Med Chem Lett·2009
7-preclinical
Matrix metalloprotease polymorphisms are associated with gas transfer in alpha 1 antitrypsin deficiency.
PMID 19293200·Ther Adv Respir Dis·2009
4-observational
Lack of agreement between arterial and central venous blood glucose measurement in critically ill children.
PMID 18797845·Intensive Care Med·2009
8-other
Release and clinical significance of soluble CD83 in chronic lymphocytic leukemia.
PMID 19195701·Leuk Res·2009
8-other
Validation of an algorithm combining haemoglobin A(1c) and fasting plasma glucose for diagnosis of diabetes mellitus in UK and Australian populations.
PMID 19236612·Diabet Med·2009
4-observational
Exubera inhaled insulin in patients with type 1 and type 2 diabetes: the first 12 months.
PMID 19580355·Diabetes Technol Ther·2009
8-other
Prediction of cure and risk of hypothyroidism in patients receiving 131I for hyperthyroidism.
PMID 18462261·Clin Endocrinol (Oxf)·2009
8-other
Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease.
PMID 19244275·Hum Mol Genet·2009
8-other
Genetic developments in autoimmune thyroid disease: an evolutionary process.
PMID 18081880·Clin Endocrinol (Oxf)·2008
6-review
Patients' perceptions of subcutaneous insulin in the OPTIMIZE study: a multicenter follow-up study.
PMID 18275360·Diabetes Technol Ther·2008
4-observational
Phenotypic differences in alpha 1 antitrypsin-deficient sibling pairs may relate to genetic variation.
PMID 19353349·COPD·2008
8-other
The TNFalpha gene relates to clinical phenotype in alpha-1-antitrypsin deficiency.
PMID 18620570·Respir Res·2008
8-other
Analysis of HLA class II genes in Hashimoto's thyroiditis reveals differences compared to Graves' disease.
PMID 18449200·Genes Immun·2008
8-other
Delayed initiation of subcutaneous insulin therapy after failure of oral glucose-lowering agents in patients with Type 2 diabetes: a population-based analysis in the UK.
PMID 18042083·Diabet Med·2007
8-other
Association of PTPN22 haplotypes with Graves' disease.
PMID 17148556·J Clin Endocrinol Metab·2007
8-other
Preliminary evidence for interaction of PTPN12 polymorphism with TSHR genotype and association with Graves' ophthalmopathy.
PMID 17608818·Clin Endocrinol (Oxf)·2007
8-other
Association of the interleukin-2 receptor alpha (IL-2Ralpha)/CD25 gene region with Graves' disease using a multilocus test and tag SNPs.
PMID 17371467·Clin Endocrinol (Oxf)·2007
4-observational
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.
PMID 17952073·Nat Genet·2007
2-rct
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 326 MORGAN ST STE D
HARKER HEIGHTS, TX 76548 - Phone
- (254) 724-2585
Quick Facts
- NPI
- 1750554374
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile