Dr. Lloyd G Goldfarb M.D.
Pulmonologist | Pulmonary Disease
227 Granite Run Dr Suite 110 Lancaster PA, 17601About
Dr. Lloyd Goldfarb practices Pulmonology in Lancaster, PA. A pulmonologist is a physician who possesses specialized knowledge and skill in the diagnosis and treatment of pulmonary conditions and diseases. Dr. Goldfarb manages patients who need life support and mechanical ventilation, and is specially trained in diseases and conditions of the chest, particularly pneumonia, asthma, tuberculosis, emphysema, and complicated chest infections.
Education and Training
Mt Sinai Sch of Med of The City Univ of Ny, New York Ny 1978
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM- Critical Care Medicine
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.
- Novel exon 3B proteolipid protein gene mutation causing late-onset spastic paraplegia type 2 with variable penetrance in female family members.
- Novel PRNP sequence variant associated with familial encephalopathy.
- Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in
- A three-sister sibship of Gerstmann-Sträussler-Scheinker disease with a CJD phenotype.
- Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.
- Inherited prion encephalopathy associated with the novel PRNP H187R mutation: a clinical study.
- Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS).
- Desmin splice variants causing cardiac and skeletal myopathy.
- Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype.
- Gluten sensitivity in sporadic and hereditary cerebellar ataxia.
- Identification and functional characterization of a novel ryanodine receptor mutation causing malignant hyperthermia in North American and South American families.
- Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry disease.
- Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutation.
- Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation.
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