Pages that link to "Q84950325"
The following pages link to Clinical Features of Autosomal Dominant and Sex-linked Ichthyosis in an English Population (Q84950325):
Displaying 50 items.
- Interventions for congenital ichthyosis (Q24194413) (← links)
- X-linked ichthyosis and X-linked placental sulfatase deficiency: a disease entity. Histochemical observations (Q24682630) (← links)
- Recent advances in understanding ichthyosis pathogenesis (Q26740640) (← links)
- The Regulation of Steroid Action by Sulfation and Desulfation (Q26799364) (← links)
- Filaggrin in the frontline: role in skin barrier function and disease (Q28242202) (← links)
- Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis (Q28303063) (← links)
- Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children. (Q33903373) (← links)
- Carrier identification by FISH analysis in isolated cases of X-linked ichthyosis (Q34085360) (← links)
- Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2. (Q34145298) (← links)
- Hereditary and acquired ichthyosis vulgaris (Q34192159) (← links)
- Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris. (Q34489270) (← links)
- The ichthyoses. Pathophysiological models of epidermal differentiation (Q34556543) (← links)
- X-linked icthyosis. A sulphatase deficiency (Q34987418) (← links)
- Placental steroid deficiency: association with arylsulfatase A deficiency (Q35202242) (← links)
- Discriminant function analysis of phenotype variates in ichthyosis (Q35231631) (← links)
- Linkage studies on X-linked ichthyosis in Sardinia (Q35231809) (← links)
- One remarkable molecule: filaggrin. (Q36043328) (← links)
- Netherton's syndrome (Q36061813) (← links)
- Bilateral lower extremity hyperkeratotic plaques: a case report of ichthyosis vulgaris (Q36078308) (← links)
- A de novo variant in the ASPRV1 gene in a dog with ichthyosis. (Q36294118) (← links)
- Disorders of keratinisation: from rare to common genetic diseases of skin and other epithelial tissues. (Q36809911) (← links)
- Pre-Descemet corneal dystrophy and X-linked ichthyosis associated with deletion of Xp22.31 containing the STS gene (Q37086498) (← links)
- Prevalence of inherited ichthyosis in France: a study using capture-recapture method (Q37479854) (← links)
- Ichthyosis vulgaris: the filaggrin mutation disease. (Q38072741) (← links)
- Enzymatic basis of typical X-linked icthyosis (Q39507731) (← links)
- Neonatal dermatology. II. Blistering and scaling dermatoses (Q39893164) (← links)
- X-linked ichthyosis: A metabolic disease (Q39904823) (← links)
- Clinical spectrum of steroid sulfatase deficiency: X-linked recessive ichthyosis, birth complications and cryptorchidism (Q40090712) (← links)
- The ichthyoses—a review (Q40106184) (← links)
- The Ichthyoses-Pathogenesis and Prenatal Diagnosis: A Review of Recent Advances (Q40111985) (← links)
- Review: genetics of steroid sulphatase deficiency and X-linked ichthyosis (Q40267834) (← links)
- Steroid sulfatase deficiency and x-linked ichthyosis (Q40636530) (← links)
- A syndrome of ichthyosis, hepatosplenomegaly and cerebellar degeneration (Q41607146) (← links)
- Overexpression of constitutively active BMP-receptor-IB in mouse skin causes an ichthyosis-vulgaris-like disease. (Q41661456) (← links)
- Ichthyosis nigricans: Ultrastructural study of the melanin pigmentary disturbances (Q41721989) (← links)
- A family with X-linked ichthyosis and hypogonadism (Q41912907) (← links)
- A collodion baby (Q42112158) (← links)
- Genetic Implications of Oculocutaneous Disorders (Q43093412) (← links)
- Ultrastructural study of the occurrence of autosomal dominant ichthyosis vulgaris in atopic eczema (Q44534860) (← links)
- Clinical pathologic correlation of superficial corneal opacities in X-linked ichthyosis. (Q45086240) (← links)
- Recombinant filaggrin is internalized and processed to correct filaggrin deficiency (Q45169364) (← links)
- Out-patient treatment of ichthyosis: a double-blind trial of ointments (Q45209972) (← links)
- X-linked ichthyosis: linkage relationship with the Xg blood groups and other studies in a large Dutch kindred (Q45857803) (← links)
- Congenital ichthyosis patient with squamous cell carcinoma of the skin who received concurrent chemoradiation: A case report. (Q55082683) (← links)
- X-linked ichthyosis in southern Italy★ (Q57244504) (← links)
- Filaggrin null mutations and childhood atopic eczema: A population-based case-control study (Q57316218) (← links)
- Filaggrin mutations p.R501X and c.2282del4 in ichthyosis vulgaris (Q57636998) (← links)
- Dominant ichthyosis vulgaris with an ultrastructuraally normal granular layer (Q67434802) (← links)
- Follow-up of a family group suffering from ichthyosis hystrix type Curth-Macklin (Q69380512) (← links)
- Absence of testicular steroid sulphatase activity in a boy with recessive X-linked ichthyosis and testicular maldescent (Q69871407) (← links)