Results 101 to 110 of about 14,024 (212)

Polyarteritis Nodosa Related with Influenza Vaccine [PDF]

, 2013
RESUMEN: Las vasculitis pueden ser secundarias a diferentes procesos, entre ellos infecciones, neoplasias, enfermedades del tejido conectivo o medicamentos, o primarias, generalmente idiopáticas.
Vásquez Duque, Gloria María, González Naranjo, Luis Alonso, Restrepo Escobar, Mauricio   +2 more
core  

Histopathological Confirmation of Axonal Sprouting in Regenerative Peripheral Nerve Interface

Plastic and Reconstructive Surgery, Global Open
Summary:. Symptomatic neuroma represents a debilitating complication after major limb amputation. The regenerative peripheral nerve interface (RPNI) has emerged as a reproducible and practical surgery aimed at mitigating the formation of painful neuroma.
Song Ho Chang, MD, PhD, Yuji Maenohara, MD, PhD, Jun Hirose, MD, PhD, Yasunori Omata, MD, PhD, Sayaka Fujiwara, MD, PhD, Nobuhiko Haga, MD, PhD, Masako Ikemura, MD, PhD, Taku Saito, MD, PhD, Sakae Tanaka, MD, PhD, Takumi Matsumoto, MD, PhD   +9 more
doaj   +1 more source

Deficiency of ADA2 (DADA2)

Güncel Pediatri
Deficiency of Adenosine Deaminase 2 (DADA2) is a systemic disorder that is inherited in an autosomal recessive manner. Initially identified as a monogenic form of systemic vasculitis that mirrors polyarteritis nodosa (PAN), DADA2 is attributed to ...
Hülya Köse, Sara Şebnem Kılıç
doaj   +1 more source

Polyarteritis Nodosa and Hydronephrosis [PDF]

Proceedings of the Royal Society of Medicine, 1958
G S, WAKEFIELD, E G, BYWATERS, R, RAMSAY
openaire   +2 more sources

Classic polyarteritis nodosa in childhood

, 2007
Polyarteritis nodosa (PAN) is a medium-sized vessel vasculitis that usually occurs in 40-60 years of age. It is a rare multisystemic disease that is frequently associated with cutaneous manifestation. It rarely occurs in childhood.
Nandi Mousomi, Maiti Arunasis, Roy Alok, Ghosh Sanat   +3 more
core  

An Unusual Presentation of Polyarteritis Nodosa: A Case Report

, 2006
Polyarteritis nodosa with gallbladder involvement is a rare condition. Autosomal dominant polycystic kidney disease is also a rare condition and rarely complicated.
E Bulbuloglu, IT Kale, T Sahinkanat, H Ciralik, M Yuksel, B Kantarceken   +5 more
core  

Persistant abdominal pain: Familial Mediterranean Fever associated with polyarteritis nodosa

, 2003
Familyal Akdeniz Ateşi, tekrarlayıcı ateş ve poliserozit atakları ile seyreden kendi kendini sınırlayan otozomal resesif geçişli bir hastalıktır. Hastalığın Henoch-Schönlein vasküliti ve poliarteritis nodosa gibi vaskülitlerle birlikteliği nadir olmakla ...
Erkin Serdaroğlu, Pelin Ertan, Ahmet Memiş, Sevgi Mir, Alphan Cura   +4 more
core  

Isaacs syndrome associated with polyarteritis nodosa. [PDF]

BMJ Case Rep
Aubry L, Badoux T, Reygaerts T, Grandmaison G.   +3 more
europepmc   +1 more source

Current and future advances in practice: polyarteritis nodosa and related vasculitides. [PDF]

Rheumatol Adv Pract
Watts RA.
europepmc   +1 more source

Rare Systemic Vasculitides: Polyarteritis Nodosa and Takayasu Arteritis. [PDF]

Am J Case Rep
Almeida R, Cereta EDS, Brasil Soares LG, Moraes MZ, Husein RAMM.   +4 more
europepmc   +1 more source