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Items: 1 to 20 of 5762

1.

Immunohistochemical evaluation of epidermal proliferation, differentiation and melanocytic density in symmetrical acrokeratoderma.

Yang PP, Peng J, Wu YY, Liu Z, Sheng P, Zhou Y, Li SJ, Fan YM.

Clin Exp Dermatol. 2017 May 22. doi: 10.1111/ced.13118. [Epub ahead of print]

PMID:
28543665
2.

Clinical, Biochemical, and Genetic Aspects of Sjögren-Larsson Syndrome.

Cho KH, Shim SH, Kim M.

Clin Genet. 2017 May 23. doi: 10.1111/cge.13058. [Epub ahead of print] Review.

PMID:
28543186
3.

[Collodion baby: clinical aspects and role of prenatal diagnosis].

Fatnassi R, Marouen N, Ragmoun H, Marzougui L, Hammami S.

Pan Afr Med J. 2017 Mar 2;26:118. doi: 10.11604/pamj.2017.26.118.10025. eCollection 2017. French.

4.

A child with epidermolytic ichthyosis from a parent with epidermolytic nevus: risk evaluation of transmission from mosaic to germline.

Kono M, Suga Y, Akashi T, Ito Y, Takeichi T, Muro Y, Akiyama M.

J Invest Dermatol. 2017 May 17. pii: S0022-202X(17)31542-7. doi: 10.1016/j.jid.2017.04.036. [Epub ahead of print] No abstract available.

PMID:
28532675
5.

Embryonic AP1 Transcription Factor Deficiency Causes a Collodion Baby-Like Phenotype.

Young CA, Eckert RL, Adhikary G, Crumrine D, Elias PM, Blumenberg M, Rorke EA.

J Invest Dermatol. 2017 May 16. pii: S0022-202X(17)31533-6. doi: 10.1016/j.jid.2017.04.032. [Epub ahead of print]

PMID:
28526300
6.

Successful Treatment of Primary Cutaneous Peripheral T-Cell Lymphoma Presenting Acquired Ichthyosis with Oral Bexarotene Monotherapy.

Tanita K, Fujimura T, Sato Y, Hidaka T, Furudate S, Kambayashi Y, Tsukada A, Hashimoto A, Aiba S.

Case Rep Oncol. 2017 Apr 6;10(1):328-332. doi: 10.1159/000468981. eCollection 2017 Jan-Apr.

7.

Autosomal Recessive Congenital Ichthyosis.

Richard G.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2001 Jan 10 [updated 2017 May 18].

8.

Distribution of ELOVL4 in the Developing and Adult Mouse Brain.

Sherry DM, Hopiavuori BR, Stiles MA, Rahman NS, Ozan KG, Deak F, Agbaga MP, Anderson RE.

Front Neuroanat. 2017 May 1;11:38. doi: 10.3389/fnana.2017.00038. eCollection 2017.

9.

MRI in neutral lipid storage disease (NLSD).

Garibaldi M, Tasca G, Diaz-Manera J, Ottaviani P, Laschena F, Pantoli D, Gerevini S, Fiorillo C, Maggi L, Tasca E, D'Amico A, Musumeci O, Toscano A, Bruno C, Massa R, Angelini C, Bertini E, Antonini G, Pennisi EM.

J Neurol. 2017 May 13. doi: 10.1007/s00415-017-8498-8. [Epub ahead of print]

PMID:
28503705
10.

Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients.

Pennisi EM, Arca M, Bertini E, Bruno C, Cassandrini D, D'amico A, Garibaldi M, Gragnani F, Maggi L, Massa R, Missaglia S, Morandi L, Musumeci O, Pegoraro E, Rastelli E, Santorelli FM, Tasca E, Tavian D, Toscano A, Angelini C; Italian NLSD Group..

Orphanet J Rare Dis. 2017 May 12;12(1):90. doi: 10.1186/s13023-017-0646-9.

11.

BJD Research Letter: A profile of lipid dysregulation in Harlequin Ichthyosis.

Ip SCI, Cottle DL, Jones LK, Weir JM, Kelsell DP, O'Toole EA, Meikle PJ, Smyth IM.

Br J Dermatol. 2017 May 10. doi: 10.1111/bjd.15642. [Epub ahead of print]

PMID:
28493316
12.

Helen Ollendorff Curth: A dermatologist's lasting legacy.

Guzman AK, James WD.

Int J Womens Dermatol. 2017 Feb 16;3(1 Suppl):S70-S74. doi: 10.1016/j.ijwd.2017.02.015. eCollection 2017 Mar. No abstract available.

13.

Acral self-healing collodion baby: A case series.

Ferrari B, Martínez JP, Luna PC, Larralde M.

Int J Womens Dermatol. 2016 Nov 9;2(4):140-142. doi: 10.1016/j.ijwd.2016.09.004. eCollection 2016 Dec.

14.

Helen Ollendorff-Curth: A dermatologist's lasting legacy.

Guzman AK, James WD.

Int J Womens Dermatol. 2016 Jul 18;2(3):108-112. doi: 10.1016/j.ijwd.2016.06.002. eCollection 2016 Sep. No abstract available.

15.

[ANALYSIS OF ONE-CARBON METABOLISM GENES AND EPIDERMAL DIFFERENTIATION COMPLEX IN PATIENTS WITH ICHTHYOSIS VULGARIS].

Fedota O, Roshchenyuk L, Sadovnychenko I, Merenkova I, Gontar I, Vorontsov V.

Georgian Med News. 2017 Mar;(264):90-97. Russian.

PMID:
28480858
16.

Nutritional Deficiency and Acquired Ichthyosis.

Holzman SB, Durso SC.

J Gen Intern Med. 2017 May 3. doi: 10.1007/s11606-017-4070-6. [Epub ahead of print] No abstract available.

PMID:
28470548
17.

Filaggrin gene polymorphism associated with Epstein-Barr virus-associated tumors in China.

Yang Y, Liu W, Zhao Z, Zhang Y, Xiao H, Luo B.

Virus Genes. 2017 Apr 28. doi: 10.1007/s11262-017-1463-x. [Epub ahead of print]

PMID:
28455573
18.

MECHANISMS IN ENDOCRINOLOGY: Update on PathoGENESis of Primary Adrenal Insufficiency - Beyond steroid enzyme deficiency and autoimmune adrenal destruction.

Flueck C.

Eur J Endocrinol. 2017 Apr 27. pii: EJE-17-0128. doi: 10.1530/EJE-17-0128. [Epub ahead of print]

PMID:
28450305
19.

Measuring the impact of dermatological conditions on family and caregivers: a review of dermatology-specific instruments.

Sampogna F, Finlay AY, Salek SS, Chernyshov P, Dalgard FJ, Evers AWM, Linder D, Manolache L, Marron SE, Poot F, Spillekom-van Koulil S, Svensson Å, Szepietowski JC, Tomas-Aragones L, Abeni D; European Academy of Dermatology and Venereology TaskForce on Quality of Life..

J Eur Acad Dermatol Venereol. 2017 Apr 20. doi: 10.1111/jdv.14288. [Epub ahead of print] Review.

PMID:
28426906
20.

What's new with common genetic skin disorders?

Ma JE, Hand JL.

Minerva Pediatr. 2017 Apr 20. doi: 10.23736/S0026-4946.17.04925-8. [Epub ahead of print]

PMID:
28425690

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