Detalhe da pesquisa
1.
Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants.
Exp Dermatol
; 33(4): e15072, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38576105
2.
A chronic fatigue syndrome model demonstrates mechanical allodynia and muscular hyperalgesia via spinal microglial activation.
Glia
; 62(9): 1407-17, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24852223
3.
Odontogenic keratocysts are an important clue for diagnosing basal cell nevus syndrome.
Nagoya J Med Sci
; 83(2): 393-396, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-34239189
4.
Plucked scalp hair follicle samples are useful RNA sources for mRNA analysis of most genodermatosis-associated genes.
J Dermatol Sci
; 111(2): 68-70, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37355462
5.
Extremely mild dominant dystrophic epidermolysis bullosa: Genotype information from whole-exome sequencing of salivary gDNA predicts disease severity.
J Dermatol
; 49(8): e276-e277, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35451103
6.
Identification of a novel causative mutation in KRT1 in diffuse palmoplantar keratoderma, facilitated by whole-exome sequencing.
Eur J Dermatol
; 31(2): 264-265, 2021 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33871364