Overview
Karolina Stepien practices practicing medicine in Salford, United Kingdom.
Ms. Stepien is highly rated in 28 conditions, according to our data. Her clinical expertise encompasses Classic Galactosemia, Mucopolysaccharidoses (MPS), Enlarged Liver, Gastrostomy, and Liver Transplant.
She is actively involved in clinical research, co-authoring 118 peer reviewed articles.
Gender
Female
Locations
Stott Lane, Salford, ENG, United Kingdom
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.
Frequently Asked Questions about Karolina M. Stepien
Is Karolina M. Stepien a top-rated expert for Classic Galactosemia?
MediFind is an objective health platform that identifies experts based on real-world data. Karolina M. Stepien is classified as an Distinguished expert for Classic Galactosemia, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Karolina M. Stepien participate in research or clinical trials?
Yes. Karolina M. Stepien has published 118 articles and abstracts on conditions like Classic Galactosemia. You can view a list of Karolina M. Stepien's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
Find Ms. Stepien's expertise for a condition
ConditionClose
- Distinguished
- Argininosuccinic AciduriaMs. Stepien isDistinguished. Learn about Argininosuccinic Aciduria.
- Classic GalactosemiaMs. Stepien isDistinguished. Learn about Classic Galactosemia.
- Enlarged LiverMs. Stepien isDistinguished. Learn about Enlarged Liver.
- FucosidosisMs. Stepien isDistinguished. Learn about Fucosidosis.
- Galactokinase DeficiencyMs. Stepien isDistinguished. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Stepien isDistinguished. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Stepien isDistinguished. Learn about Galactosemia.
- Mucopolysaccharidoses (MPS)Ms. Stepien isDistinguished. Learn about Mucopolysaccharidoses (MPS).
- Ornithine Transcarbamylase DeficiencyMs. Stepien isDistinguished. Learn about Ornithine Transcarbamylase Deficiency.
- Phosphomannoisomerase DeficiencyMs. Stepien isDistinguished. Learn about Phosphomannoisomerase Deficiency.
- Urea Cycle Disorders (UCD)Ms. Stepien isDistinguished. Learn about Urea Cycle Disorders (UCD).
View All 11 Distinguished Conditions
- Advanced
- Alpha MannosidosisMs. Stepien isAdvanced. Learn about Alpha Mannosidosis.
- Arginase DeficiencyMs. Stepien isAdvanced. Learn about Arginase Deficiency.
- Brachydactyly Mononen TypeMs. Stepien isAdvanced. Learn about Brachydactyly Mononen Type.
- Carnitine Palmitoyltransferase 2 Deficiency
- Fabry DiseaseMs. Stepien isAdvanced. Learn about Fabry Disease.
- Familial Glucocorticoid DeficiencyMs. Stepien isAdvanced. Learn about Familial Glucocorticoid Deficiency.
- Fumarase DeficiencyMs. Stepien isAdvanced. Learn about Fumarase Deficiency.
- Gaucher DiseaseMs. Stepien isAdvanced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Ms. Stepien isAdvanced. Learn about Gaucher Disease Type 1.
- HomocystinuriaMs. Stepien isAdvanced. Learn about Homocystinuria.
- Homocystinuria due to MTHFR Deficiency
- Methylmalonic Acidemia with Homocystinuria
- MPI-CDGMs. Stepien isAdvanced. Learn about MPI-CDG.
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- RhabdomyolysisMs. Stepien isAdvanced. Learn about Rhabdomyolysis.
- SplenomegalyMs. Stepien isAdvanced. Learn about Splenomegaly.
- Von Gierke DiseaseMs. Stepien isAdvanced. Learn about Von Gierke Disease.
View All 17 Advanced Conditions
- Experienced
- Absence SeizureMs. Stepien isExperienced. Learn about Absence Seizure.
- Acid Sphingomyelinase Deficiency (ASMD)Ms. Stepien isExperienced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- AgranulocytosisMs. Stepien isExperienced. Learn about Agranulocytosis.
- AlkaptonuriaMs. Stepien isExperienced. Learn about Alkaptonuria.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- CardiomyopathyMs. Stepien isExperienced. Learn about Cardiomyopathy.
- Carnitine Palmitoyltransferase 1 Deficiency
- CataractMs. Stepien isExperienced. Learn about Cataract.
- Chanarin-Dorfman SyndromeMs. Stepien isExperienced. Learn about Chanarin-Dorfman Syndrome.
- CholestasisMs. Stepien isExperienced. Learn about Cholestasis.
- Chronic Kidney DiseaseMs. Stepien isExperienced. Learn about Chronic Kidney Disease.
- Congenital Adrenal Hyperplasia (CAH)Ms. Stepien isExperienced. Learn about Congenital Adrenal Hyperplasia (CAH).
- CystinosisMs. Stepien isExperienced. Learn about Cystinosis.
- Drug Induced DyskinesiaMs. Stepien isExperienced. Learn about Drug Induced Dyskinesia.
- Ectopic Cushing's syndromeMs. Stepien isExperienced. Learn about Ectopic Cushing's syndrome.
- ErythromelalgiaMs. Stepien isExperienced. Learn about Erythromelalgia.
- Farber LipogranulomatosisMs. Stepien isExperienced. Learn about Farber Lipogranulomatosis.
- GangliosidosisMs. Stepien isExperienced. Learn about Gangliosidosis.
- GastrostomyMs. Stepien isExperienced. Learn about Gastrostomy.
- Generalized Tonic-Clonic SeizureMs. Stepien isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- Glycogen Storage Disease Type 3Ms. Stepien isExperienced. Learn about Glycogen Storage Disease Type 3.
- Glycogen Storage Disease Type 9Ms. Stepien isExperienced. Learn about Glycogen Storage Disease Type 9.
- GM1 GangliosidosisMs. Stepien isExperienced. Learn about GM1 Gangliosidosis.
- Gyrate Atrophy of the Choroid and RetinaMs. Stepien isExperienced. Learn about Gyrate Atrophy of the Choroid and Retina.
- Hearing LossMs. Stepien isExperienced. Learn about Hearing Loss.
- Hepatocerebral DegenerationMs. Stepien isExperienced. Learn about Hepatocerebral Degeneration.
- High Blood Pressure in InfantsMs. Stepien isExperienced. Learn about High Blood Pressure in Infants.
- HistiocytosisMs. Stepien isExperienced. Learn about Histiocytosis.
- Hormone Replacement Therapy (HRT)Ms. Stepien isExperienced. Learn about Hormone Replacement Therapy (HRT).
- HypogonadismMs. Stepien isExperienced. Learn about Hypogonadism.
- Hypogonadotropic HypogonadismMs. Stepien isExperienced. Learn about Hypogonadotropic Hypogonadism.
- HypothyroidismMs. Stepien isExperienced. Learn about Hypothyroidism.
- HypotoniaMs. Stepien isExperienced. Learn about Hypotonia.
- Infantile NeutropeniaMs. Stepien isExperienced. Learn about Infantile Neutropenia.
- Infantile Refsum DiseaseMs. Stepien isExperienced. Learn about Infantile Refsum Disease.
- IntersexMs. Stepien isExperienced. Learn about Intersex.
- Isolated Hypogonadotropic HypogonadismMs. Stepien isExperienced. Learn about Isolated Hypogonadotropic Hypogonadism.
- Krabbe DiseaseMs. Stepien isExperienced. Learn about Krabbe Disease.
- Liver TransplantMs. Stepien isExperienced. Learn about Liver Transplant.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- MalnutritionMs. Stepien isExperienced. Learn about Malnutrition.
- Methylmalonic AcidemiaMs. Stepien isExperienced. Learn about Methylmalonic Acidemia.
- Mitochondrial Trifunctional Protein Deficiency
- Mononeuritis MultiplexMs. Stepien isExperienced. Learn about Mononeuritis Multiplex.
- Mucolipidosis 3Ms. Stepien isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Ms. Stepien isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Multiple Sulfatase DeficiencyMs. Stepien isExperienced. Learn about Multiple Sulfatase Deficiency.
- NeuralgiaMs. Stepien isExperienced. Learn about Neuralgia.
- Niemann-Pick DiseaseMs. Stepien isExperienced. Learn about Niemann-Pick Disease.
- Non-Langerhans-Cell HistiocytosisMs. Stepien isExperienced. Learn about Non-Langerhans-Cell Histiocytosis.
- OchronosisMs. Stepien isExperienced. Learn about Ochronosis.
- OsteoporosisMs. Stepien isExperienced. Learn about Osteoporosis.
- ParaplegiaMs. Stepien isExperienced. Learn about Paraplegia.
- Phenylketonuria (PKU)Ms. Stepien isExperienced. Learn about Phenylketonuria (PKU).
- PMM2-Congenital Disorder of GlycosylationMs. Stepien isExperienced. Learn about PMM2-Congenital Disorder of Glycosylation.
- Pompe DiseaseMs. Stepien isExperienced. Learn about Pompe Disease.
- Refsum DiseaseMs. Stepien isExperienced. Learn about Refsum Disease.
- ReticulohistiocytomaMs. Stepien isExperienced. Learn about Reticulohistiocytoma.
- SeizuresMs. Stepien isExperienced. Learn about Seizures.
- SialidosisMs. Stepien isExperienced. Learn about Sialidosis.
- SpasticityMs. Stepien isExperienced. Learn about Spasticity.
- Tay-Sachs DiseaseMs. Stepien isExperienced. Learn about Tay-Sachs Disease.
- Vitamin B12 Deficiency AnemiaMs. Stepien isExperienced. Learn about Vitamin B12 Deficiency Anemia.
- Wilson DiseaseMs. Stepien isExperienced. Learn about Wilson Disease.
View All 67 Experienced Conditions
Want to save this expert for later?
Not sure about your diagnosis?
Are you the provider on this profile?