Ramot Y - Search Results

1

Generalized verrucosis and HPV-3 susceptibility associated with CD4 T-cell lymphopenia caused by inherited human interleukin-7 deficiency.

Horev L, Unger S, Molho-Pessach V, Meir T, Maly A, Stepensky P, Zamir M, Keller B, Babay S, Warnatz K, Ramot Y, Zlotogorski A. Horev L, et al. Among authors: ramot y. J Am Acad Dermatol. 2015 Jun;72(6):1082-4. doi: 10.1016/j.jaad.2015.02.1118. J Am Acad Dermatol. 2015. PMID: 25981006 No abstract available.

2

Endocrine controls of keratin expression.

Ramot Y, Paus R, Tiede S, Zlotogorski A. Ramot Y, et al. Bioessays. 2009 Apr;31(4):389-99. doi: 10.1002/bies.200800121. Bioessays. 2009. PMID: 19274655 Review.

3

Inflammatory and chloracne-like skin lesions in B6C3F1 mice exposed to 3,3',4,4'-tetrachloroazobenzene for 2 years.

Ramot Y, Nyska A, Lieuallen W, Maly A, Flake G, Kissling GE, Brix A, Malarkey DE, Hooth MJ. Ramot Y, et al. Toxicology. 2009 Nov 9;265(1-2):1-9. doi: 10.1016/j.tox.2009.08.017. Epub 2009 Sep 6. Toxicology. 2009. PMID: 19737593 Free PMC article.

4

Diabetes mellitus may be the earliest and sole manifestation of the H syndrome.

Broshtilova V, Ramot Y, Molho-Pessach V, Zlotogorski A. Broshtilova V, et al. Among authors: ramot y. Diabet Med. 2009 Nov;26(11):1179-80. doi: 10.1111/j.1464-5491.2009.02843.x. Diabet Med. 2009. PMID: 19929999 No abstract available.

5

Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript.

Ramot Y, Horev L, Smolovich I, Molho-Pessach V, Zlotogorski A. Ramot Y, et al. Exp Dermatol. 2010 Aug;19(8):e320-2. doi: 10.1111/j.1600-0625.2009.01042.x. Exp Dermatol. 2010. PMID: 20163456 Free article.

6

Early-onset sensorineural hearing loss is a prominent feature of H syndrome.

Ramot Y, Sayama K, Sheffer R, Doviner V, Hiller N, Kaufmann-Yehezkely M, Zlotogorski A. Ramot Y, et al. Int J Pediatr Otorhinolaryngol. 2010 Jul;74(7):825-7. doi: 10.1016/j.ijporl.2010.03.053. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20399510

7

Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome: a case report.

Ramot Y, Czarnowicki T, Maly A, Navon-Elkan P, Zlotogorski A. Ramot Y, et al. Pediatr Dermatol. 2011 Sep-Oct;28(5):538-41. doi: 10.1111/j.1525-1470.2010.01163.x. Epub 2010 Jun 9. Pediatr Dermatol. 2011. PMID: 20553399

8

Finasteride induced Gynecomastia: Case report and Review of the Literature.

Ramot Y, Czarnowicki T, Zlotogorski A. Ramot Y, et al. Int J Trichology. 2009 Jan;1(1):27-9. doi: 10.4103/0974-7753.51930. Int J Trichology. 2009. PMID: 20805972 Free PMC article.

9

Mutations in two genes on chromosome 13 resulting in a complex hair and skin phenotype due to two rare genodermatoses: KLICK and autosomal recessive woolly hair/hypotrichosis simplex.

Horev L, Babay S, Ramot Y, Saad-Edin B, Moorad S, Ingber A, Maly A, Zlotogorski A. Horev L, et al. Among authors: ramot y. Br J Dermatol. 2011 May;164(5):1113-6. doi: 10.1111/j.1365-2133.2011.10229.x. Br J Dermatol. 2011. PMID: 21275938 No abstract available.

10

An extraordinary colocalization of alopecia areata and vitiligo.

Ramot Y, Thomaidou E, Mali A, Zlotogorski A. Ramot Y, et al. Int J Trichology. 2010 Jul;2(2):108-9. doi: 10.4103/0974-7753.77522. Int J Trichology. 2010. PMID: 21712899 Free PMC article.

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