Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlationHAMADA, Takahiro; WESSAGOWIT, Vesarat; LENANE, Patsy et al.Journal of investigative dermatology. 2003, Vol 120, Num 3, pp 345-350, issn 0022-202X, 6 p.Article

A novel homozygous 62-bp insertion in ECM1 causes lipoid proteinosis in a multigeneration Pakistani familyNASIR, M; LATIF, A; AJMAL, M et al.British journal of dermatology (1951). 2009, Vol 161, Num 3, pp 688-690, issn 0007-0963, 3 p.Article

Hyalinosis cutis et mucosae: a 30 year follow up of a female patientBRAJAC, Ines; KASTELAN, Marija; GRUBER, Franjo et al.EJD. European journal of dermatology. 2004, Vol 14, Num 5, pp 310-313, issn 1167-1122, 4 p.Article

Lipoid proteinosis in two familiesKUCHABAL, Shankarling D; KUCHABAL, Deekappa S.International journal of dermatology. 2011, Vol 50, Num 8, pp 972-975, issn 0011-9059, 4 p.Article

Prominent corneal nerves: a novel sign of lipoid proteinosisAL-FAKY, Yasser H; BOSLEY, Thomas M; AL-TURKI, Turki et al.British journal of ophthalmology. 2012, Vol 96, Num 7, pp 935-940, issn 0007-1161, 6 p.Article

Clinical and molecular characterization of lipoid proteinosis in Namaqualand, South AfricaVAN HOUGENHOUCK-TULLEKEN, W; CHAN, I; HAMADA, T et al.British journal of dermatology (1951). 2004, Vol 151, Num 2, pp 413-423, issn 0007-0963, 11 p.Article

Clinical and molecular abnormalities in lipoid proteinosisDESMET, S; DEVOS, S. A; CHAN, I et al.EJD. European journal of dermatology. 2005, Vol 15, Num 5, pp 344-346, issn 1167-1122, 3 p.Article

Lipoid proteinosis : A report of 2 siblings and a brief review of the literatureAL-NATOUR, Sahar H.Saudi medical journal. 2008, Vol 29, Num 8, pp 1188-1191, issn 0379-5284, 4 p.Article

Lipoid proteinosis in two brothers with multiple organ involvement from Saudi ArabiaAL-BITAR, Yasser; AZAM JAH SAMDANI.International journal of dermatology. 2004, Vol 43, Num 5, pp 360-361, issn 0011-9059, 2 p.Article

A novel missense mutation of the ECM1 gene in a Chinese patient with lipoid proteinosisLIU, W; XU, W; YANG, X et al.Clinical and experimental dermatology (Print). 2012, Vol 37, Num 1, pp 28-30, issn 0307-6938, 3 p.Article

The Neuropsychiatry and Neuropsychology Of Lipoid ProteinosisTHORNTON, Helena B; NEL, Daan; THORNTON, Dorothy et al.The Journal of neuropsychiatry and clinical neurosciences. 2008, Vol 20, Num 1, pp 86-92, issn 0895-0172, 7 p.Article

Lipoid proteinosis: a case reportGALADARI, I; AL-KUWAITI, R.International journal of dermatology. 2004, Vol 43, Num 5, pp 368-370, issn 0011-9059, 3 p.Article

A case of oral recurrent ulcerative lesions in a patient with lipoid proteinosis (Urbach-Wiethe disease)SARGENTI, Sergio; DANTAS BATISTA, Jonas; DURIGHETTO, Antônio Francisco et al.British journal of oral & maxillofacial surgery. 2010, Vol 48, Num 8, pp 654-655, issn 0266-4356, 2 p.Article

Free-floating desmosomes in lipoid proteinosis : An inherent defect in keratinocyte adhesion?DYER, Jon A; YU, Qian-Chun; PALLER, Amy S et al.Pediatric dermatology. 2006, Vol 23, Num 1, pp 1-6, issn 0736-8046, 6 p.Article

New compound heterozygous mutations in a Chinese family with lipoid proteinosisWANG, C. Y; ZHANG, P. Z; ZHANG, F. R et al.British journal of dermatology (1951). 2006, Vol 155, Num 2, pp 470-472, issn 0007-0963, 3 p.Article

Primary diagnosis of hyalinosis cutis et mucosae in a 56-year-old man with persistent hoarseness and dysphoniaLANG, Sabrina C; GLAS, Sophie; SCHEICH, Matthias et al.EJD. European journal of dermatology. 2013, Vol 23, Num 2, pp 272-273, issn 1167-1122, 2 p.Article

Molecular basis of lipoid proteinosis in a Libyan familyCHAN, I; EL-ZURGHANY, A; ZENDAH, B et al.Clinical and experimental dermatology (Print). 2003, Vol 28, Num 5, pp 545-548, issn 0307-6938, 4 p.Article

Belastungsabhängige Dysphonie, rezidivierende Pleuropneumonie und supraglottische Raumforderung = Pressure-related dysphonia, recurring pneumonia and supraglottic tumorJAHN, K; STRAEHLER-POHL, H.-J; FISCHER, H.-R et al.HNO. Hals-, Nasen-, Ohrenärzte. 2010, Vol 58, Num 9, pp 931-933, issn 0017-6192, 3 p.Article

SPONTANEOUS INTRACEREBRAL HEMORRHAGE IN URBACH-WIETHE DISEASEMESSINA, Maria Josè; NUZZACO, Graziamaria; BARBIERI, Alessandra et al.Neurology. 2012, Vol 79, Num 16, pp 1740-1741, issn 0028-3878, 2 p.Article

Should we think of Urbach: Wiethe disease in refractory epilepsy? Case report and review of the literatureHOSSEIN GHELICHNIA OMRANI; TAJDINI, Masih; GHELICHNIA, Babak et al.Journal of the neurological sciences. 2012, Vol 320, Num 1-2, pp 149-152, issn 0022-510X, 4 p.Article

A failure of mucocutaneous lymphangiogenesis may underlie the clinical features of lipoid proteinosisUCHIDA, T; HAYASHI, H; INAOKI, M et al.British journal of dermatology (1951). 2007, Vol 156, Num 1, pp 152-157, issn 0007-0963, 6 p.Article

Functional redundancy of extracellular matrix protein 1 in epidermal differentiationSERCU, S; POUMAY, Y; HERPHELIN, F et al.British journal of dermatology (1951). 2007, Vol 157, Num 4, pp 771-775, issn 0007-0963, 5 p.Article

The molecular basis of lipoid proteinosis : mutations in extracellular matrix protein 1LEN CHAN; LU LIU; HAMADA, Takahiro et al.Experimental dermatology. 2007, Vol 16, Num 11, pp 881-890, issn 0906-6705, 10 p.Article

Lipoid proteinosis in siblingsAGRAWAL, Sanjay N.Indian Journal of Dermatology Venereology and Leprology. 2003, Vol 69, Num 2, pp 71-72, issn 0378-6323, 2 p., SUP1Article

Vesicular lesions in a patient with lipoid proteinosis: A probable acantholytic dermatosisKO, Christine; BARR, Ronald J.The American journal of dermatopathology. 2003, Vol 25, Num 4, pp 335-337, issn 0193-1091, 3 p.Article