Keywords: ژنودرماتوز; Dermatoscopia; Entodermatoscopia; Inflamoscopia; Tricoscopia; Alopecias cicatriciales; Alopecias no cicatriciales; Distrofias pilosas genéticas; Tumores cutáneos benignos acrómicos; Tumores vasculares; Trastornos pigmentarios; Genodermatosis;
مقالات ISI ژنودرماتوز (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: ژنودرماتوز; Mosaicismo; LÃneas de Blaschko; Dermatosis lineal; Hamartoma; Nevo; Genodermatosis; Liquen estriado; Blaschkitis; Inactivación del cromosoma X (lyonización); mutación poscigótica.;
Keywords: ژنودرماتوز; Genodermatosis; Epidermolysis bullosa; Epidermolysis bullosa simplex; Epidermolysis bullosa junctional; Epidermolysis bullosa dystrophic; Kindler syndrome; Genetic diagnosis; Antigen mapping; Prenatal diagnosis; Preimplantation diagnosis; Genodermatosis;
Keywords: ژنودرماتوز; genodermatosis; Buschke-Ollendorff Syndrome; Ichthyosis hystrix Curth-Macklin type; Curth's criteria; Ollendorff probe sign;
Keywords: ژنودرماتوز; autoinflammation; autoinflammatory; gangrene; genodermatosis; inflammation; interferonopathy; interstitial lung disease; vasculitis; IFN; interferon; JAK; Janus kinase; NIH; National Institutes of Health; SAVI; stimulator of interferon genes-associated
Keywords: ژنودرماتوز; genodermatosis; Buschke-Ollendorff Syndrome; Ichthyosis hystrix Curth-Macklin type; Curth's criteria; Ollendorff probe sign;
Keywords: ژنودرماتوز; ACTH; adrenocorticotropic hormone; ADAM10; a disintegrin and metalloprotease 10; ADAR; adenosine deaminase acting on RNA; AP1/3; adaptor protein 1/3; BLOC1-3; biogenesis of lysosome-related organelles complex 1-3; DCT; dopachrome tautomerase; DSRAD; dou
Keywords: ژنودرماتوز; Enfermedad de Darier; Genodermatosis; Gen ATP2A2; Proteína SERCA2; Enfermedad acantolítica; Disqueratosis; Retinoides
Keywords: ژنودرماتوز; Fibroma; Angioma; Leiomioma; Schwannoma; Neurofibroma; Genodermatosis
A case of subungual tumors of incontinentia pigmenti: A rare manifestation and association with bipolar disease
Keywords: ژنودرماتوز; bipolar disorder; Bloch-Sulzberger syndrome; genodermatosis; IKBKG; incontinentia pigmenti; lines of Blaschko; NEMO; NF-kappa-B; psychiatric disease; subungual tumors of incontinentia pigmenti; IP; incontinentia pigmenti; NF-κB; nuclear factor-κB; STIPs
Early-onset stroke, polyarteritis nodosa (PAN), and livedo racemosa
Keywords: ژنودرماتوز; deficiency of adenosine deaminase 2; genodermatosis; livedo; polyarteritis nodosa; stroke; ADA2; adenosine deaminase 2; CECR1; cat eye syndrome chromosome region, candidate 1; CVA; cerebrovascular accidents; DADA2; deficiency of adenosine deaminase 2; NIH
Ptbp1 and Exosc9 knockdowns trigger skin stability defects through different pathways
Keywords: ژنودرماتوز; RNA-binding proteins; Genodermatosis; Post-transcriptional regulations; Epidermis;
Japanese recurrent mutation c.6216Â +Â 5GÂ >Â T in COL7A1 leads to a mild phenotype of dystrophic epidermolysis bullosa
Keywords: ژنودرماتوز; Recurrent mutation; Splice site mutation; Type VII collagen; Skin blistering; Genodermatosis;
Splicing abnormality of integrin β4 gene (ITGB4) due to nucleotide substitutions far from splice site underlies pyloric atresia-junctional epidermolysis bullosa syndrome
Keywords: ژنودرماتوز; Genodermatosis; Blister; Branch-point mutation; Splice site mutation; RT-PCR
Estrategias terapéuticas innovadoras para la epidermólisis bullosa distrófica recesiva
Keywords: ژنودرماتوز; Genodermatosis; Epidermólisis bullosa; Terapias avanzadas; GenéticaGenodermatosis; Epidermolysis bullosa; Advanced therapies; Genetics
Gene expression profiling in pachyonychia congenita skin
Keywords: ژنودرماتوز; Painful palmoplantar keratoderma; Genodermatosis; Monogenic skin disorder; mTOR signaling pathway; Keratinocyte; Desquamation
Advances in the therapeutic use of mammalian target of rapamycin (mTOR) inhibitors in dermatology
Keywords: ژنودرماتوز; antiproliferative; autoimmune; drug repurposing; genodermatosis; immunosuppression; inflammatory; mammalian target of rapamycin; neoplasia; percutaneous therapy; rapamycin; sirolimus; vascular anomaliesAkt, protein kinase B; BHD, Birt-Hogg-Dubé syndrome;
Esclerosis tuberosa de Bourneville
Keywords: ژنودرماتوز; Esclerosis tuberosa de Bourneville; Genodermatosis; Hamartoma; Angiofibromas; Astrocitomas de células gigantes; mTOR;
H syndrome: The first 79 patients
Keywords: ژنودرماتوز; genodermatosis; H syndrome; histiocytosis; hyperpigmentation; SLC29A3; FHS; familial histiocytosis syndrome; IDDM; insulin-dependent diabetes mellitus; OMIM; online Mendelian inheritance in man; PHID; pigmented hypertrichosis with insulin-dependent diabet
Dyschromatosis symmetrica hereditaria: A retrospective case series and literature review
Keywords: ژنودرماتوز; ADAR1 gene; dyschromatosis symmetrica hereditaria; genodermatosis; Taiwanese
IQoL-32: A new ichthyosis-specific measure of quality of life
Keywords: ژنودرماتوز; genodermatosis; ichthyosis; quality of life; questionnaire; score; toolANIPS, Association Nationale des Ichtyoses et Peaux Sèches pathologiques; DLQI, Dermatology Life Quality Index; QoL, quality of life; SF-12, Short Form-12 health-related questionnaire
Poroqueratosis
Keywords: ژنودرماتوز; Poroqueratosis; Laminilla cornoide; Genodermatosis; Queratinización; Inmunosupresión;
The spectrum of radiological findings in H syndrome
Keywords: ژنودرماتوز; Computed tomography; Imaging; Genodermatosis; H-syndrome
Displasias ectodérmicas: revisión clÃnica y molecular
Keywords: ژنودرماتوز; Genodermatosis; Displasia ectodérmica; Factor Nuclear kappa B; Ectodisplasina; ProteÃna p63; Genodermatosis; Ectodermal dysplasia; Nuclear Factor kappa B; Ectodysplasin; Protein p63;
Ectodermal Dysplasias: A Clinical and Molecular Review
Keywords: ژنودرماتوز; Genodermatosis; Ectodermal dysplasia; Nuclear Factor kappa B; Ectodysplasin; Protein p63Genodermatosis; Displasia ectodérmica; Factor Nuclear kappa B; Ectodisplasina; Proteína p63
Maladie de Dowling-Degos étendue après PUVA thérapie prolongée
Keywords: ژنودرماتوز; Maladie de Dowling-Degos; Génodermatose; Photothérapie; Pigmentation; Maladie de Haber; Dowling-Degos disease; Genodermatosis; PUVA therapy; Pigmentation; Haber disease;
A review of the clinical phenotype of 254 patients with genetically confirmed pachyonychia congenita
Keywords: ژنودرماتوز; genodermatosis; hyperkeratosis; keratin; keratinizing disorder; keratoderma; pachyonychia congenitaIPCRR, International Pachyonychia Congenita Research Registry; OR, odds ratio; PC, pachyonychia congenita
Cutis laxa: A review
Keywords: ژنودرماتوز; cutis laxa; elastic tissue; elastin; fibulin-4; fibulin-5; genodermatosis; ACL; acquired cutis laxa; ADCL; autosomal dominant cutis laxa; ARCL; autosomal recessive cutis laxa; ATS; arterial tortuosity syndrome; CL; cutis laxa; DBS; De Barsy syndrome; EDS;
Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations
Keywords: ژنودرماتوز; Genodermatosis; Genetic modifier; Skin barrier; Eczema; Ichthyosis
Dyschromatosis universalis hereditaria: a familial case with ultrastructural skin investigation
Keywords: ژنودرماتوز; dyschromatosis; genodermatosis; melanocyte; melanosome
rAAV2-mediated restoration of LEKTI in LEKTI-deficient cells from Netherton patients
Keywords: ژنودرماتوز; Genodermatosis; Cutaneous gene therapy; Serine protease; Cornified envelope; Adeno-associated virus
The immigration delay disease: Adermatoglyphia–inherited absence of epidermal ridges
Keywords: ژنودرماتوز; adermatoglyphia; embryology; epidermal ridges; fingerprints; genodermatosis; morphogenesis
Risk of squamous cell carcinoma in junctional epidermolysis bullosa, non-Herlitz type: Report of 7 cases and a review of the literature
Keywords: ژنودرماتوز; collagen type XVII; epidermolysis bullosa; genodermatosis; laminin-332; skin cancer; squamous cell carcinomaEB, epidermolysis bullosa; EBS, epidermolysis bullosa simplex; JEB, junctional epidermolysis bullosa; JEB-nH, junctional epidermolysis bullosa, typ
Síndromes esclerodermiformes y estados seudoesclerodérmicos
Keywords: ژنودرماتوز; Síndrome esclerodermiforme; Estado seudoesclerodérmico; Genodermatosis; Escleromixedema; Fibrosis sistémica nefrogénica; Escleroedema de Buschke; Síndrome POEMS; Amilosis primaria; Reacción crónica injerto contra huésped; Lipodermatoesclerosis; Síndrome c
Syndrome de Conradi-Hünermann-Happle de disposition unilatérale
Keywords: ژنودرماتوز; Chondrodysplasie ponctuée dominante liée à l'X; Génodermatose; Calcifications ponctuées épiphysaires; Gène EBP; Syndrome de Conradi-Hünermann-Happle; X-linked dominant chondrodysplasia punctata; Genodermatosis; Punctuate epiphyseal calcification
Kindler Syndrome Pathogenesis and Fermitin Family Homologue 1 (Kindlin-1) Function
Keywords: ژنودرماتوز; Genodermatosis; Keratinocyte adhesion; Keratinocyte proliferation; Signaling; Focal contact; Fermitin family homologue 1 (FFH1); Ultrastructure;
Genitourinary Tract Involvement in Epidermolysis Bullosa
Keywords: ژنودرماتوز; Blister; Genodermatosis; Urethral stenosis; Hydronephrosis; Renal failure;
Lethal Acantholytic Epidermolysis Bullosa
Keywords: ژنودرماتوز; Desmoplakin; Keratin; Keratinocyte; Skin fragility; Desmosome; Genodermatosis;
Ectodermal Dysplasia-Skin Fragility Syndrome
Keywords: ژنودرماتوز; Desmosome; Cell adhesion; Blister; Keratinocyte; Genodermatosis;
X-linked ichthyosis: An oculocutaneous genodermatosis
Keywords: ژنودرماتوز; genodermatosis; hyperkeratosis; ichthyosis; X-linked
Prenatal Diagnosis of Epidermolysis Bullosa
Keywords: ژنودرماتوز; Genodermatosis; Fetal skin biopsy; Chorionic villus sampling; Preimplantation genetic diagnosis; Noninvasive prenatal testing;
Hair follicle-specific keratins and their diseases
Keywords: ژنودرماتوز; Genodermatosis; Mutation; Monilethrix; Loose anagen hair; Ectodermal dysplasia; Inner root sheath; Companion layer; Review
Skin manifestations of systemic disease
Keywords: ژنودرماتوز; acanthosis nigricans; cutaneous lupus; dermatomyositis; erythema nodosum; flushing; genodermatosis; morphoea; necrobiosis lipoidica; paraneoplastic dermatoses; pretibial myxoedema; pyoderma gangrenosum; sarcoidosis
Quoi de neuf en dermatologie pédiatrique ?
Keywords: ژنودرماتوز; Dermatite atopique; Hémangiome; Naevus congénital; Verrue; Génodermatose; Atopic dermatitis; Haemangioma; Congenital naevus; Wart; Genodermatosis;
Genotype-phenotype correlation in non-Hallopeau-Siemens recessive dystrophic epidermolysis bullosa: The splice site mutation c.6216Â +Â 5GÂ >Â T in the COL7A1 gene results in aberrant and normal splicings
Keywords: ژنودرماتوز; Anchoring fibrils; Genodermatosis; Premature termination codon; Type VII collagen;
Cutaneous gene delivery
Keywords: ژنودرماتوز; Gene therapy; Barrier function; Genodermatosis
A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita
Keywords: ژنودرماتوز; Keratoderma; Genodermatosis; Keratinizing disorder; Nail dystrophy; Bullous disease
Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis
Keywords: ژنودرماتوز; Filaggrin; eczema; ichthyosis; keratinization; skin barrier; atopy; skin; genodermatosis; genetics; mutationAD, Atopic dermatitis; DMSO, Dimethyl sulfoxide; EDC, Epidermal differentiation complex; IV, Ichthyosis vulgaris
Genética molecular en dermatologÃa
Keywords: ژنودرماتوز; Genética; DermatologÃa; Mutaciones; Genodermatosis;
Quoi de neuf en dermatologie pédiatrique ?
Keywords: ژنودرماتوز; Dermatologie pédiatrique; Dermatite atopique; Génodermatose; Maladies auto-immunes de l'enfant; Pediatric dermatology diseases; Genodermatosis; Atopic eczema; Angiomas; Pediatric auto-immune diseases;