SG Kant, HJ van der Kamp, M Kriek… - Journal of Clinical …, 2011 - Endocrine Soc ... The Jumping SHOX Gene—Crossover in the Pseudoautosomal Region Resulting in Unusual Inheritance of Leri-Weill Dyschondrosteosis. ... The classic clinical triad in Leri-Weill dyschondrosteosis (LWD) is short stature, mesomelia, and Madelung deformity. ... Cited by 4 - Related articles - All 3 versions
P Anversa, J Kajstura, A Leri… - Nature Medicine, 2011 - nature.com ...Leri, A., Kajstura, J. & Anversa, P. Physiol. Rev. 85, 1373–1416 (2005). ... Annarosa Leri. Search for this author in: ...
S Benito-Sanz, E Barroso, D Heine-Suñer… - Journal of Clinical …, 2011 - Endocrine Soc ... Institution: Google Indexer | Sign In via User Name/Password The Journal of Clinical Endocrinology ...Leri A, Weill J 1929 Une affection congenitale et symetrique du developpement osseux: la dyschondrosteose. Bull Mem Soc Med Hop ... Cited by 2 - Related articles - All 4 versions
A Hajjioui, H Khazzani, S Sbihi, R Bahiri… - Annals of physical and …, 2011 - Elsevier ... At the clinical examination we find a positive Leri'ssign on the right side with tactile hypoesthesia and epicritic sensibility in the right L4 nerve root, no motor deficit or lumbar spine syndrome. The rest of the examination is eventless. There is no biological inflammatory syndrome. ... Related articles - All 3 versions
JM Wit, W Kiess… - … Practice & Research Clinical Endocrinology & …, 2011 - Elsevier ... 22 On this radiograph also indications can be found for other disorders, such as a Madelung deformity as sign of Leri–Weill dyschondrosteosis (SHOX defect). If body proportions are abnormal, a full skeletal survey is indicated, as recently reviewed. [*3] , [4] and [*13]. ... Cited by 1 - Related articles - All 4 versions
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