Results 101 to 110 of about 4,869,361 (145)

Very Rare Case of Hyaline Fibromatosis Syndrome Successfully Treated with Surgical Excision and Review of Literature. [PDF]

Arch Plast Surg
Jung YU, Kim BJ, Kim EH.
europepmc   +1 more source

Lipoid Proteinosis: A Rare Case Report and Review of Literature. [PDF]

Indian Dermatol Online J
Verma D, Mendiratta V, Yadav V, Birla A, Srivastava A.   +4 more
europepmc   +1 more source

Lipoid proteinosis: A rare genodermatosis with multisystemic manifestations-A case report. [PDF]

Clin Case Rep
Hashmi FN, Huma S, Singireddy H, Zareen N, Suvvari TK, Ansari MH, Sultana N, Hasibuzzaman MA.   +7 more
europepmc   +1 more source

Myocardial Growth Response to Fetal Intralipid Infusion in Sheep. [PDF]

FASEB J
Iverson K, McClellan EB, Jonker SS, Louey S.   +3 more
europepmc   +1 more source

Hyperacute silicosis after bronchoscopy-induced melanoptysis in a lung transplant patient. A first report in literature. [PDF]

Interdiscip Cardiovasc Thorac Surg
Saenz A, Dreyse J, Melo J, Giglio A.
europepmc   +1 more source

Lipoid proteinosis: Urbach-Wiethe disease

Acta Paediatrica, 1993
Lipoid proteinosis (Urbach‐Wicthe disease) is a rare autosomal recessive disorder in which hyalinized material is deposited in the skin, mucous membranes and brain. Laryngeal changes resulting in hoarseness may be present at birth or in early infancy, often being the first sign of the discase. A typical case is presented.
Cinaz P., Güvenir T., Gönlügen G.
core   +6 more sources

Some of the next articles are maybe not open access.

Related searches:

Study of the lipids in the skin lesions in urbach-wiethe disease

Clinica Chimica Acta, 1977
A patient with Urbach-Wiethe disease was studied, with special attention given to the analysis of the skin and mucosal lesions. An eosinophilia in the peripheral blood and a diabetic tendency were found. The skin papules and mucosal plaques contain abundant lipids, especially cholesterol (66 percent) and phospholipids (27 percent).
J Valles, M T Santos, J Aznar
exaly   +3 more sources

Marathon of eponyms: 21 Urbach-Wiethe disease (Lipoid proteinosis)

Oral Diseases, 2011
Oral Diseases (2011) 17, 729–730The use of eponyms has long been contentious, but many remain in common use, as discussed elsewhere (Editorial: Oral Diseases. 2009: 15; 185). The use of eponyms in diseases of the head and neck is found mainly in specialties dealing with medically compromised individuals (paediatric dentistry, special care dentistry ...
J Langdon
exaly   +3 more sources

Urbach-Wiethe Disease

2009
Gudrun Rappold, John-John B. Schnog, Victor E. A. Gerdes, Yvonne G. Weber, Jose M. Serratosa, Anna-Elina Lehesjoki, Alessandra Baumer, André B. P. Kuilenburg, Albert H. Gennip*, David C. Rees, Lynette D. Fairbanks, H. Anne Simmonds, Albrecht Hesse, Albrecht Hesse, Diana J. Zimmermann, Gerd E. Von Unruh, Bernd Hoppe, Roswitha Siener, Albrecht Hesse, Naim M. Maalouf, MaryAnn Cameron, Khashayar Sakhaee, Alexander K. C. Leung, Susan Kupka, Markus Pfister, Nikolaos E. Bechrakis, Henry J. Kaplan, Hui Shao, Deming Sun   +28 more
exaly   +2 more sources

Lipoid Proteinosis (Urbach-Wiethe Disease)

Ophthalmologica, 1999
The aim of this study has been to assess the clinical presentation and biochemical profile of lipoid proteinosis within a defined pedigree. Glycoprotein analysis was compared to normal values in an attempt to define a biochemical phenotype. Six affected family members were identified with variable degrees of disease expression.
Costagliola C, Verolino M, Landolfo P, Winkler NR, MASTROPASQUA, Leonardo, Landolfo V.   +5 more
openaire   +6 more sources