SKELETAL PAIN IN CHILDREN: DON’T FORGET SCURVY! A PAEDIATRIC CASE SERIES

Autor: Alessandra Di Nora

Publikováno v: Euromediterranean Biomedical Journal, Vol 18, Iss 13, Pp 64-67 (2023)

Appropriate nutritional intake is an important aspect in children’s overall health. In developed countries, malnutrition is related to chronic illness or restrictive dietary habits, related to psychiatric or behavioural conditions such as anorexia

Externí odkaz: https://doaj.org/article/144529947fe94b98946a02806be1e482

Piezo2 Knockdown Inhibits Noxious Mechanical Stimulation and NGF-Induced Sensitization in A-Delta Bone Afferent Neurons

Autor: Sara Nencini, Michael Morgan, Jenny Thai, Andrew I. Jobling, Stuart B. Mazzone, Jason J. Ivanusic

Publikováno v: Frontiers in Physiology, Vol 12 (2021)

Piezo2 is a mechanically gated ion-channel that has a well-defined role in innocuous mechanical sensitivity, but recently has also been suggested to play a role in mechanically induced pain. Here we have explored a role for Piezo2 in mechanically evo

Externí odkaz: https://doaj.org/article/8b33c2abbe6a4312bb79fef7be7bb105

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Frequency of Vitamin D Deficiency in Common Musculo Skeletal Conditions

Autor: Behzad Heidari, Parham Heidari, Elham Samari, Moazameh Ramzannia Jalali

Publikováno v: Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, Vol 16, Iss 12, Pp 7-15 (2014)

BACKGROUND AND OBJECTIVE: Vitamin D deficiency is an important known responsible factor for development,progression and exacerbation of many musculoskeletal disease.The aim of the present study was to determine the status of serum vitamin D in a numb

Externí odkaz: https://doaj.org/article/efd9701e6a3d4f65b189afd32d55c2a1

Excellent response to asfotase alfa treatment in an adolescent patient with hypophosphatasia

Autor: Elsebet Ostergaard, Allan M. Lund, Olivia Sarah Strandbech

Publikováno v: JIMD Reports
Strandbech, O S, Lund, A & Ostergaard, E 2021, ' Excellent response to asfotase alfa treatment in an adolescent patient with hypophosphatasia ', JIMD Reports, vol. 59, no. 1, pp. 10-15 . https://doi.org/10.1002/jmd2.12198
JIMD Reports, Vol 59, Iss 1, Pp 10-15 (2021)

Hypophosphatasia (HPP) is a rare inherited metabolic disorder characterized by deficient activity of alkaline phosphatase, causing defective mineralization of bones and teeth. The symptoms vary from no symptoms to stillbirth or skeletal manifestation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66062c70b00dd99705da881c1f4194ef
http://europepmc.org/articles/PMC8100395