Results 141 to 150 of about 5,744 (198)

Ehlers-Danlos Syndrome: A Tale of Two Cases Highlighting Rare Subtypes and Diagnostic Considerations. [PDF]

Cureus
Pati K, Tripathy SR, Patnaik SS, Parida MK, Das BK.   +4 more
europepmc   +1 more source

Surgical management of Nutcracker syndrome caused by a middle mesenteric artery in an adolescent. [PDF]

J Vasc Surg Cases Innov Tech
Bori Bata AK, Metchihoungbe S, Ibrahim A, Lafia KT, Kouomboua PSM, Ahounou E.   +5 more
europepmc   +1 more source

Hauerwas and Disability Law: Exposing the Cracks in the Foundations of Disability Law [PDF]

, 2012
Schiltz, Elizabeth R.
core   +1 more source

Nonamyloidogenic TTR gene variants c.76G>A and c.337-18G>C are not associated with idiopathic small-fiber neuropathy. [PDF]

Eur J Neurol
Konecki C, Francou B, Chappell K, Augey L, Beaudonnet G, Cauquil C, Dimitri-Boulos D, Not A, Adam C, Poinsignon V, Verstuyft C, Adams D, Echaniz-Laguna A, Labeyrie C.   +13 more
europepmc   +1 more source

Significant Microvascular Abnormalities Present in Autonomic Nervous System Dysfunction: Results of a Cross-Sectional Study. [PDF]

Biomedicines
Mumtaz S, Arca K, Majithia V, Cheshire W, Hodge D, Berianu F.   +5 more
europepmc   +1 more source

An Emerging Population: The Chronically Critically Ill [PDF]

, 2014
Jurasinski, Philip, Schindler, Christine A.   +1 more
core   +1 more source

Progressive Spastic Paraparesis as the Dominant Manifestation of Adolescent-Onset Alexander Disease: Case Report and Literature Review. [PDF]

J Clin Med
Smółka KA, Smółka L, Guz W, Chaber E, Perenc L.   +4 more
europepmc   +1 more source

New Challenges and Perspectives in Neurology and Autonomic Disorders: A Leap Forward. [PDF]

J Pers Med
Blitshteyn S, Ruhoy I.
europepmc   +1 more source

Multiple System Atrophy (Cerebellar Type) With Overlapping Progressive Muscular Atrophy Features and Genetic Erb-B2 Receptor Tyrosine Kinase 4 (ERBB4) Amyotrophic Lateral Sclerosis Variant: A Case Report. [PDF]

Cureus
Panganiban ELC, Rosales RL.
europepmc   +1 more source