El Hachem M - Search Results

1

Hoarse cry in a newborn with epidermolysis bullosa simplex, generalized severe.

Diociaiuti A, Giancristoforo S, Pisaneschi E, Condorelli AG, Boldrini R, Zambruno G, El Hachem M. Diociaiuti A, et al. Among authors: el hachem m. Pediatr Dermatol. 2020 Mar;37(2):393-395. doi: 10.1111/pde.14105. Epub 2020 Jan 19. Pediatr Dermatol. 2020. PMID: 31957133

2

Laminin-5 mutational analysis in an Italian cohort of patients with junctional epidermolysis bullosa.

Posteraro P, De Luca N, Meneguzzi G, El Hachem M, Angelo C, Gobello T, Tadini G, Zambruno G, Castiglia D. Posteraro P, et al. Among authors: el hachem m. J Invest Dermatol. 2004 Oct;123(4):639-48. doi: 10.1111/j.0022-202X.2004.23302.x. J Invest Dermatol. 2004. PMID: 15373767 Free article.

3

Necrosis of the tongue as first symptom of Polyarteritis Nodosa (PAN): unusual presentation of a rare disease in children.

Buonuomo PS, El Hachem M, Callea F, Bracaglia C, Diociaiuti A, Pardeo M, Campana A, Insalaco A, Cortis E, Ugazio AG. Buonuomo PS, et al. Among authors: el hachem m. Rheumatol Int. 2013 Apr;33(4):1071-3. doi: 10.1007/s00296-010-1642-8. Epub 2010 Dec 7. Rheumatol Int. 2013. PMID: 21136262

4

Esophageal stenosis in epidermolysis bullosum: a challenge for the endoscopist.

De Angelis P, Caldaro T, Torroni F, Romeo E, Foschia F, di Abriola GF, Rea F, El Hachem M, Genovese E, D'Alessandro S, Dall'Oglio L. De Angelis P, et al. Among authors: el hachem m. J Pediatr Surg. 2011 May;46(5):842-7. doi: 10.1016/j.jpedsurg.2011.02.017. J Pediatr Surg. 2011. PMID: 21616238

5

Proteolytic activation cascade of the Netherton syndrome-defective protein, LEKTI, in the epidermis: implications for skin homeostasis.

Fortugno P, Bresciani A, Paolini C, Pazzagli C, El Hachem M, D'Alessio M, Zambruno G. Fortugno P, et al. Among authors: el hachem m. J Invest Dermatol. 2011 Nov;131(11):2223-32. doi: 10.1038/jid.2011.174. Epub 2011 Jun 23. J Invest Dermatol. 2011. PMID: 21697885 Free article.

6

Long-term follow-up of a spontaneously improving patient with junctional epidermolysis bullosa associated with ITGB4 c.3977-19T>A splicing mutation.

Diociaiuti A, Castiglia D, Morini F, Boldrini R, Fortugno P, Zambruno G, El Hachem M. Diociaiuti A, et al. Among authors: el hachem m. Acta Derm Venereol. 2013 Jan;93(1):116-8. doi: 10.2340/00015555-1381. Acta Derm Venereol. 2013. PMID: 22674212 Free article. No abstract available.

7

The 420K LEKTI variant alters LEKTI proteolytic activation and results in protease deregulation: implications for atopic dermatitis.

Fortugno P, Furio L, Teson M, Berretti M, El Hachem M, Zambruno G, Hovnanian A, D'Alessio M. Fortugno P, et al. Among authors: el hachem m. Hum Mol Genet. 2012 Oct 1;21(19):4187-200. doi: 10.1093/hmg/dds243. Epub 2012 Jun 23. Hum Mol Genet. 2012. PMID: 22730493

8

Impressive pseudotumoral proliferative nodules in a giant congenital nevus of a newborn.

Palmieri G, Bianciardi Valassina MF, Proia G, El Hachem M, Callea F, Zama M. Palmieri G, et al. Among authors: el hachem m. Pediatr Dermatol. 2013 May-Jun;30(3):e5-7. doi: 10.1111/j.1525-1470.2012.01845.x. Epub 2012 Sep 7. Pediatr Dermatol. 2013. PMID: 22958141

9

Lethal Netherton syndrome due to homozygous p.Arg371X mutation in SPINK5.

Diociaiuti A, Castiglia D, Fortugno P, Bartuli A, Pascucci M, Zambruno G, El Hachem M. Diociaiuti A, et al. Among authors: el hachem m. Pediatr Dermatol. 2013 Jul-Aug;30(4):e65-7. doi: 10.1111/pde.12076. Epub 2013 Jan 17. Pediatr Dermatol. 2013. PMID: 23331056

10

Congenital myxoid and pigmented dermatofibrosarcoma protuberans: a case report.

El Hachem M, Diociaiuti A, Latella E, Zama M, Lambiase C, Giraldi L, Surrenti T, Callea F. El Hachem M, et al. Pediatr Dermatol. 2013 Sep-Oct;30(5):e74-7. doi: 10.1111/pde.12131. Epub 2013 Mar 28. Pediatr Dermatol. 2013. PMID: 23534369

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