Results 161 to 170 of about 3,300 (212)

Multiple Pulmonary Cavernous Hemangioma: A Case Report. [PDF]

Surg Case Rep
Takashima S, Nanjo H, Matsuo T, Kuriyama S, Iwai H, Suzuki H, Kobayashi M, Fujibayashi T, Shibano S, Minamiya Y, Imai K.   +10 more
europepmc   +1 more source

Middle meningeal artery embolization and tranexamic acid therapy for subdural hematoma in a patient with hereditary hemorrhagic telangiectasia: illustrative case. [PDF]

J Neurosurg Case Lessons
Kushmakov R, Cazorla-Morales I, Brenner K, Araten D, Shapiro M, Raz E, Placantonakis DG.   +6 more
europepmc   +1 more source

A Rare Case of Intracranial Hemorrhage Mimicking a Neoplasm in a Child With Hereditary Hemorrhagic Telangiectasia. [PDF]

Cureus
Solano C, Silva G, VerHage TR, Chandra T, Bajaj M.   +4 more
europepmc   +1 more source

A diagnostic approach to neurocutaneous syndromes. [PDF]

Arq Neuropsiquiatr
Gama SM, Tamanini JVG, Moraes MPM, Silva TYT, Lima FT, Pedroso JL, Barsottini OGP.   +6 more
europepmc   +1 more source

Rendu-Osler-Weber: γονότυπος και φαινότυπος

, 2014
openaire   +1 more source

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Hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease)

Lancet, The, 2003
Correspondence to: Dr Uichiro Fuchizaki, Keiju Medical Center, 94 Tomioka-cho, Nanao, Ishikawa 926-8605, Japan (e-mail: fuchi@p1.coralnet.or.jp) Hereditary haemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber disease, is an autosomal dominant disorder characterised by epistaxis, cutaneous telangiectasia (figure 3), and visceral ...
Uichiro, Fuchizaki, Hirotoshi, Miyamori, Shunsuke, Kitagawa, Shuichi, Kaneko, Kenichi, Kobayashi   +4 more
exaly   +3 more sources

Rendu-Osler-Weber syndrome

BMJ, 2014
A 55 year old man presented with recurrent epistaxis and no risk factors or family history. Examination showed extensive telangiectasia on his nasal …
A. Banigo, G. MacDougall
openaire   +1 more source

Rendu-Osler-Weber disease: update of medical and dental considerations

Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, 2008
Rendu-Osler-Weber disease, also known as hereditary hemorrhagic telangiectasia (HHT), is an autosomal dominant inherited disorder characterized by an aberrant vascular development. The reported prevalence is approximately 1 per 5,000-10,000. The clinical manifestations consist of recurrent spontaneous nosebleeds, telangiectasias characteristically at ...
te Veldhuis, E.C., te Veldhuis, A.H., van Dijk, F.S., Kwee, M.L., van Hagen, J.M., Baart, J.A., van der Waal, I.   +6 more
openaire   +4 more sources