Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tracy Kornafel"'
Autor:
Can Ficicioglu, Dena R. Matalon, Nicole Luongo, Caitlin Menello, Tracy Kornafel, Andrew J. Degnan
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Abstract Background Mucopolysaccharidosis (MPS) IVA, also known as Morquio A syndrome, is a rare autosomal recessive lysosomal storage disorder caused by a deficiency in the enzyme N-acetylgalactosamine-6-sulfatase. Early recognition, diagnosis, and
Externí odkaz:
https://doaj.org/article/4047ccdb58bb47e39d51151b229030e1
Publikováno v:
Developmental scienceREFERENCES.
We investigated the role of rate limiting factors in development using walking as a model system. The achievement of bipedal posture and locomotion are among the most significant achievements in an infant's first year, with poor balance and weak musc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6946d689e143963e8b8596724a2d1312
https://pubmed.ncbi.nlm.nih.gov/35593750
https://pubmed.ncbi.nlm.nih.gov/35593750
Autor:
Amy Waldman, Tracy Kornafel, Geraldine Liu, Ann T. Harrington, Laura Adang, Samuel R. Pierce, Amanda K. Jan, Adeline Vanderver, Elizabeth Ballance, Francesco Gavazzi, Scott A. Lorch, Allan M. Glanzman, Sara B. DeMauro, Justine Shults
Publikováno v:
Pediatr Neurol
Background Leukodystrophies are a rare class of disorders characterized by severe neuromotor disability. There is a strong need for research regarding the functional status of people with leukodystrophy which is limited by the need for in-person asse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc15934b5f2fdea939d8cd9af53dd41c
https://europepmc.org/articles/PMC8629609/
https://europepmc.org/articles/PMC8629609/
Autor:
Andrew J. Degnan, Caitlin Menello, Nicole Luongo, Tracy Kornafel, Dena R. Matalon, Can Ficicioglu
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Background Mucopolysaccharidosis (MPS) IVA, also known as Morquio A syndrome, is a rare autosomal recessive lysosomal storage disorder caused by a deficiency in the enzyme N-acetylgalactosamine-6-sulfatase. Early recognition, diagnosis, and treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a98735f4be36af2a4e3f2f8d291de1c5
http://europepmc.org/articles/PMC7706253
http://europepmc.org/articles/PMC7706253
Publikováno v:
Physical & Occupational Therapy In Pediatrics. 37:485-595
The purpose of this case report is to describe the inpatient rehabilitation program of a 13-year-old boy with acute flaccid myelitis (AFM), specific to physical and occupational therapy examination, treatment, and outcomes.AFM is a rare, acute neurol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cee9ff26a1aa99d56303e77ed471ab0
https://doi.org/10.1080/01942638.2016.1255289
https://doi.org/10.1080/01942638.2016.1255289
Publikováno v:
Developmental neurorehabilitation. 23(2)
Purpose: The purpose of this research was to investigate differences in Early Clinical Assessment of Balance (ECAB) scores within children with cerebral palsy (CP) with different Gross Motor Function Classification System (GMFCS) levels and between c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a64cfc9e827ec23083eb4d4817f59489
https://pubmed.ncbi.nlm.nih.gov/31661347
https://pubmed.ncbi.nlm.nih.gov/31661347