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  2. Our Research
  3. Anna Lehman

Anna Lehman

Associate Professor
VCH Clinical Title(s)
Medical Director, Adult Metabolic Diseases
Research Focus
Genetics
Contact Info
scholar.google.ca/citations?user=F8dvXGYAAAAJ&hl=en
anna.lehman@vch.ca
604-875-5965
Mailing Address

4th Floor, 2775 Laurel St
Vancouver BC V5Z1M9
Canada

Biography

Dr. Anna Lehman is Associate Professor in the Department of Medical Genetics at the University of British Columbia, where she also completed her training. She practices in the specialty of Inherited Metabolic Diseases at Vancouver General Hospital in the Adult Metabolic Diseases Clinic. Her research program identifies novel genetic causes of disease and seeks to improve management of genetic disorders affecting metabolism. 

Research Studies

Blood, Heart and Circulation, Genetics

Evaluating the effect of venglustat for Fabry disease

Genetics

Evaluating the long-term safety of lucerastat for Fabry disease

Brain and Nerves, Genetics

A Prospective Observational Study of Patients With Primary Mitochondrial Disease (SPIMM-300)

Publications

  • The Journal of clinical endocrinology and metabolism -

    X-Linked Hypophosphatemia Management in Adults: An International Working Group Clinical Practice Guideline.

    Khan AA, Ali DS, Appelman-Dijkstra NM, Carpenter TO, Chaussain C, Imel EA, Jan de Beur SM, Florenzano P, Abu Alrob H, Aldabagh R, Alexander RT, Alsarraf F, Beck-Nielsen SS, Biosse-Duplan M, Cohen-Solal M, Crowley RK, Dandurand K, Filler G, Friedlander L, Fukumoto S, Gagnon C, Goodyer P, Grasemann C, Grimbly C, Hussein S, Javaid MK, Khan S, Khan A, Lehman A, Lems WF, Lewiecki EM, McDonnell C, Mirza RD, Morgante E, Morrison A, Portale AA, Rhee Y, Rush ET, Siggelkow H, Tetradis S, Tosi L, Ward LM, Guyatt G, Brandi ML
  • Journal of inherited metabolic disease -

    The Frequencies of Different Inborn Errors of Metabolism in Adult Metabolic Centres: 10 Years Later, Another Report From the SSIEM Adult Metabolic Physicians Group.

    Tchan M, Lehman A, van Dussen L, Langendonk JG, Janssen MCH, Langeveld M, Murphy E, Ryder B, Glamuzina E, Merkel M, Sechi A, Arnoux JB, Mochel F, Alkemade G, Maillot F, Kaphan E, Mazodier K, Thomas Q, Leguy-Seguin V, Marelli C
  • Diabetes -

    Diabetes Associated With Maternally Inherited Diabetes and Deafness (MIDD): From Pathogenic Variant to Phenotype.

    Chanoine JP, Thompson DM, Lehman A
  • Journal of medical genetics -

    Dominant negative variants in cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay.

    Mohajeri A, Vaseghi-Shanjani M, Rosenfeld JA, Yang GX, Lu H, Sharma M, Lin S, Salman A, Waqas M, Sababi Azamian M, Worley KC, Del Bel KL, Kozak FK, Rahmanian R, Biggs CM, Hildebrand KJ, Lalani SR, Nicholas SK, Scott DA, Mostafavi S, van Karnebeek C, Henkelman E, Halparin J, Yang CL, Armstrong L, , , Turvey SE, Lehman A
  • Neurology -

    Efficacy and Safety of Elamipretide in Individuals With Primary Mitochondrial Myopathy: The MMPOWER-3 Randomized Clinical Trial.

    Karaa A, Bertini E, Carelli V, Cohen BH, Enns GM, Falk MJ, Goldstein A, Gorman GS, Haas R, Hirano M, Klopstock T, Koenig MK, Kornblum C, Lamperti C, Lehman A, Longo N, Molnar MJ, Parikh S, Phan H, Pitceathly RDS, Saneto R, Scaglia F, Servidei S, Tarnopolsky M, Toscano A, Van Hove JLK, Vissing J, Vockley J, Finman JS, Brown DA, Shiffer JA, Mancuso M,
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