Cargando…
A Novel Manifestation of Prolidase Deficiency in a Toddler Diagnosed With Very-early-onset Crohn Disease
Autores principales: | Rizvi, S. Ahsan, Elder, Melissa, Beasley, Genie |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727922/ https://www.ncbi.nlm.nih.gov/pubmed/31107408 http://dx.doi.org/10.1097/MPG.0000000000002402 |
Ejemplares similares
-
Osteoarticular Manifestations of Prolidase Deficiency and Disability: Case Reports of Two Moroccan Sisters
por: Asly, Mouna, et al.
Publicado: (2021) -
Prolidase deficiency diagnosed by whole exome sequencing in a child with pulmonary capillaritis
por: Rayment, Jonathan H., et al.
Publicado: (2019) -
Clinical Genetics of Prolidase Deficiency: An Updated Review
por: Spodenkiewicz, Marta, et al.
Publicado: (2020) -
Ulceration in Prolidase Deficiency: Successful Treatment with Anticoagulants
por: SÜßMUTH, Kira, et al.
Publicado: (2020) -
Sequential and combined treatment of prolidase deficiency leg ulcers
por: Palumbo, F P, et al.
Publicado: (2010)