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Quoted phrase not found in phrase index: "Absent keratohyalin granules"
Page 1
Histologic and immunohistochemical characteristics of cutaneous cysts in Goltz-Gorlin syndrome: clues for differentiation of nonsyndromic cysts.
Tirado M, Ständer S, Metze D. Tirado M, et al. Am J Dermatopathol. 2014 Nov;36(11):892-8. doi: 10.1097/DAD.0000000000000081. Am J Dermatopathol. 2014. PMID: 24698937
Only 2 cases showed an exclusive steatocystoma-like type of epithelium very similar to odontogenic keratocysts. Sebaceous glands and follicular structures were absent. There were no differences between palmar and plantar cysts and other anatomic locations. The ultrastructu …
Only 2 cases showed an exclusive steatocystoma-like type of epithelium very similar to odontogenic keratocysts. Sebaceous glands and follicu …
Squamous differentiation and basal lamina deposition in endometrial adenoacanthoma.
Gould VE, Sommers SC, Terzakis JA. Gould VE, et al. Am J Pathol. 1976 Jul;84(1):25-38. Am J Pathol. 1976. PMID: 945698 Free PMC article.
However, the granule population was small, with relatively scanty keratohyaline and no definite membrane coating granules. ...These observations suggest a high level of differentiation in respect to synthetic capabilities and cell surface recognition. They co …
However, the granule population was small, with relatively scanty keratohyaline and no definite membrane coating granules …
Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis.
Nomura T, Sandilands A, Akiyama M, Liao H, Evans AT, Sakai K, Ota M, Sugiura H, Yamamoto K, Sato H, Palmer CN, Smith FJ, McLean WH, Shimizu H. Nomura T, et al. J Allergy Clin Immunol. 2007 Feb;119(2):434-40. doi: 10.1016/j.jaci.2006.12.646. J Allergy Clin Immunol. 2007. PMID: 17291859
Immunohistologic and ultrastructural observations indicated that both truncation mutations lead to a striking reduction of keratohyalin granules in the epidermis. We screened 143 Japanese patients with AD for these FLG null mutations and identified them in 8 patient …
Immunohistologic and ultrastructural observations indicated that both truncation mutations lead to a striking reduction of keratohyalin …
Severe congenital generalized exfoliative erythroderma in newborns and infants: a possible sign of Netherton syndrome.
Hausser I, Anton-Lamprecht I. Hausser I, et al. Pediatr Dermatol. 1996 May-Jun;13(3):183-99. doi: 10.1111/j.1525-1470.1996.tb01202.x. Pediatr Dermatol. 1996. PMID: 8806118
Epidermal barrier function was Impaired by the highly suppressed terminal differentiation, with thin or in part completely absent stratum corneum, decrease of keratin filaments, decrease or lack of keratohyalin granules, and of keratinosomes containing stacks …
Epidermal barrier function was Impaired by the highly suppressed terminal differentiation, with thin or in part completely absent str …