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Quoted phrase not found in phrase index: "Ichthyosis, congenital, autosomal recessive 14"
Page 1
Proteomic manifestations of genetic defects in autosomal recessive congenital ichthyosis.
Karim N, Durbin-Johnson B, Rocke DM, Salemi M, Phinney BS, Naeem M, Rice RH. Karim N, et al. J Proteomics. 2019 Jun 15;201:104-109. doi: 10.1016/j.jprot.2019.04.007. Epub 2019 Apr 10. J Proteomics. 2019. PMID: 30978464 Clinical Trial.
Present work investigates the degree to which the departure from normal of ichthyosis corneocytes on the skin surface depends upon the basic defect as judged by proteomic profiling. Analyzing autosomal recessive congenital ichthyosis arising fro …
Present work investigates the degree to which the departure from normal of ichthyosis corneocytes on the skin surface depends upon th …
Effect of topical tazarotene in the treatment of congenital ichthyoses.
Hofmann B, Stege H, Ruzicka T, Lehmann P. Hofmann B, et al. Br J Dermatol. 1999 Oct;141(4):642-6. doi: 10.1046/j.1365-2133.1999.03101.x. Br J Dermatol. 1999. PMID: 10583110
Diagnoses were X-linked recessive ichthyosis, non-erythrodermic autosomal recessive lamellar ichthyosis, autosomal dominant ichthyosis vulgaris and ichthyosis bullosa of Siemens (IBS). ...Clinical and laborator …
Diagnoses were X-linked recessive ichthyosis, non-erythrodermic autosomal recessive lamellar ichthyosi …
Treatment of ichthyosis lamellaris using a series of herbal skin care products family.
Tirant M, Bayer P, Hercogovấ J, Fioranelli M, Gianfaldoni S, Chokoeva AA, Tchernev G, Wollina U, Novotny F, Roccia MG, Maximov GK, França K, Lotti T. Tirant M, et al. J Biol Regul Homeost Agents. 2016 Apr-Jun;30(2 Suppl 3):65-72. J Biol Regul Homeost Agents. 2016. PMID: 27498660 Clinical Trial.
Lamellar ichthyosis (LI) is a genetically heterogeneous group of disorders of keratinization that are inherited in an autosomal recessive fashion, occurring in approximately 1 in 300,000 live births. ...A multi-centre European prospective study was con …
Lamellar ichthyosis (LI) is a genetically heterogeneous group of disorders of keratinization that are inherited in an autos …
Experience of low-dose dexamethasone use in the respiratory management of ichthyosis prematurity syndrome.
Henderson D, Murphy CA, O'Dea M, Boyle MA. Henderson D, et al. BMJ Case Rep. 2021 Aug 20;14(8):e243348. doi: 10.1136/bcr-2021-243348. BMJ Case Rep. 2021. PMID: 34417235 Free PMC article.
Ichthyosis prematurity syndrome (IPS) is a rare disorder of autosomal recessive inheritance. ...
Ichthyosis prematurity syndrome (IPS) is a rare disorder of autosomal recessive inheritance. ...
Syndrome of ichthyosis congenita, neurosensory deafness, oligophrenia, dental aplasia, brachydactyly, clinodactyly, accessory cervical ribs and carcinoma of the thyroid.
Ruzicka T, Goerz G, Anton-Lamprecht I. Ruzicka T, et al. Dermatologica. 1981;162(2):124-36. doi: 10.1159/000250259. Dermatologica. 1981. PMID: 7250456
Further findings included dental aplasia, brachydactyly, clinodactyly and accessory cervical ribs. At the age of 14, a thyroid carcinoma was diagnosed. Therapy with a retinoid derivative (Ro 10-9359) resulted in a marked improvement of the ichthyosis. We assume a ge …
Further findings included dental aplasia, brachydactyly, clinodactyly and accessory cervical ribs. At the age of 14, a thyroid carcin …