Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/36936
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | İmren, Işıl Göğem | - |
dc.contributor.author | Tanacan, E. | - |
dc.contributor.author | Ceylaner, S. | - |
dc.contributor.author | Sumer, G. | - |
dc.contributor.author | Eksioglu, M. | - |
dc.date.accessioned | 2021-02-02T09:23:20Z | |
dc.date.available | 2021-02-02T09:23:20Z | |
dc.date.issued | 2020 | - |
dc.identifier.issn | 1396-0296 | - |
dc.identifier.uri | https://hdl.handle.net/11499/36936 | - |
dc.identifier.uri | https://doi.org/10.1111/dth.14152 | - |
dc.description.abstract | Abstract Not Available | en_US |
dc.language.iso | en | en_US |
dc.publisher | Blackwell Publishing Inc. | en_US |
dc.relation.ispartof | Dermatologic Therapy | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | emollient agent | en_US |
dc.subject | protein glutamine gamma glutamyltransferase | en_US |
dc.subject | pyroxylin | en_US |
dc.subject | transglutaminase 1 | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | acanthosis | en_US |
dc.subject | birth weight | en_US |
dc.subject | case report | en_US |
dc.subject | cephalopelvic disproportion | en_US |
dc.subject | cesarean section | en_US |
dc.subject | child | en_US |
dc.subject | clinical article | en_US |
dc.subject | clinical feature | en_US |
dc.subject | disease course | en_US |
dc.subject | epidermis | en_US |
dc.subject | follow up | en_US |
dc.subject | gene mutation | en_US |
dc.subject | genetic association | en_US |
dc.subject | gestational age | en_US |
dc.subject | histopathology | en_US |
dc.subject | homozygosity | en_US |
dc.subject | human | en_US |
dc.subject | human tissue | en_US |
dc.subject | hyperkeratosis | en_US |
dc.subject | ichthyosis | en_US |
dc.subject | lamellar ichthyosis | en_US |
dc.subject | Letter | en_US |
dc.subject | newborn | en_US |
dc.subject | preschool child | en_US |
dc.subject | punch biopsy | en_US |
dc.subject | stop codon | en_US |
dc.subject | Turkey (republic) | en_US |
dc.title | Mild lamellar ichthyosis with a truncated homozygous TGM1 mutation in a pediatric patient from Turkey | en_US |
dc.type | Letter | en_US |
dc.identifier.volume | 33 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.doi | 10.1111/dth.14152 | - |
dc.relation.publicationcategory | Diğer | en_US |
dc.identifier.pmid | 32767474 | en_US |
dc.identifier.scopus | 2-s2.0-85090218340 | en_US |
dc.identifier.wos | WOS:000566269100001 | en_US |
dc.identifier.scopusquality | Q2 | - |
dc.owner | Pamukkale University | - |
item.openairetype | Letter | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.fulltext | No Fulltext | - |
item.languageiso639-1 | en | - |
item.grantfulltext | none | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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