Overview
Agnieszka Gach practices in Lodz, Poland. Ms. Gach is rated as an Experienced expert by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Kallmann Syndrome, Familial Partial Lipodystrophy, Familial Hypercholesterolemia, and High Cholesterol.
Her clinical research consists of co-authoring 46 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Chromosome 13q Duplication.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Distinguished
- Kallmann SyndromeMs. Gach isDistinguished. Learn about Kallmann Syndrome.
- Advanced
- Familial HypercholesterolemiaMs. Gach isAdvanced. Learn about Familial Hypercholesterolemia.
- Familial HypertriglyceridemiaMs. Gach isAdvanced. Learn about Familial Hypertriglyceridemia.
- Familial Partial Lipodystrophy
- High CholesterolMs. Gach isAdvanced. Learn about High Cholesterol.
- HypogonadismMs. Gach isAdvanced. Learn about Hypogonadism.
- Hypogonadotropic HypogonadismMs. Gach isAdvanced. Learn about Hypogonadotropic Hypogonadism.
- Experienced
- Albright's Hereditary Osteodystrophy
- AnosmiaMs. Gach isExperienced. Learn about Anosmia.
- Chromosome 13q DuplicationMs. Gach isExperienced. Learn about Chromosome 13q Duplication.
- Chromosome 7p DeletionMs. Gach isExperienced. Learn about Chromosome 7p Deletion.
- Defective Apolipoprotein B-100Ms. Gach isExperienced. Learn about Defective Apolipoprotein B-100.
- Heterozygous Familial Hypercholesterolemia (HeFH)