Pages that link to "Q96156279"
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The following pages link to Christine Bodemer (Q96156279):
Displaying 50 items.
- Syndromic (phenotypic) diarrhea in early infancy (Q21202896) (← links)
- LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome (Q24314860) (← links)
- Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response (Q24338296) (← links)
- Mast cell sarcoma: new cases and literature review (Q28071802) (← links)
- Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families (Q28200896) (← links)
- Corneodesmosomal cadherins are preferential targets of stratum corneum trypsin- and chymotrypsin-like hyperactivity in Netherton syndrome (Q28235669) (← links)
- Pain and quality of life evaluation in patients with localized epidermolysis bullosa simplex (Q32186957) (← links)
- Phenotypic and genotypic characteristics of mastocytosis according to the age of onset (Q33327689) (← links)
- Clinical spectrum of tufted angiomas in childhood: a report of 13 cases and a review of the literature (Q33390857) (← links)
- Thrombotic microangiopathy and Purtscher-like retinopathy as a rare presentation of juvenile dermatomyositis (Q33399539) (← links)
- Kaposiform Haemangioendothelioma-spectrum Lesions with Kasabach-Merritt Phenomenon: Retrospective Analysis and Long-term Outcome (Q33423711) (← links)
- Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I (Q33656182) (← links)
- Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa (Q33948142) (← links)
- Chronic mucocutaneous candidiasis in humans with inborn errors of interleukin-17 immunity (Q34025875) (← links)
- Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009. (Q34126886) (← links)
- Incontinentia pigmenti and hypomelanosis of Ito. (Q34690858) (← links)
- The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes (Q34915159) (← links)
- Cutaneous EBV-related lymphoproliferative disorder in a 15-year-old boy with AIDS: an unusual clinical presentation (Q35001943) (← links)
- Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis (Q35144610) (← links)
- Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study. (Q35147055) (← links)
- New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein (Q35652037) (← links)
- Skin markers of occult spinal dysraphism in children: a review of 54 cases (Q35894307) (← links)
- A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency (Q36001303) (← links)
- X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production (Q36228741) (← links)
- Adjuvant treatment with the bacterial lysate (OM-85) improves management of atopic dermatitis: A randomized study (Q36319745) (← links)
- Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity. (Q36688645) (← links)
- Family burden in inherited ichthyosis: creation of a specific questionnaire (Q36690574) (← links)
- Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey (Q36923083) (← links)
- Importance of therapeutic patient education in ichthyosis: results of a prospective single reference center study (Q37116645) (← links)
- BRAF Mutation Correlates With High-Risk Langerhans Cell Histiocytosis and Increased Resistance to First-Line Therapy (Q37659076) (← links)
- Assessment of Type I Interferon Signaling in Pediatric Inflammatory Disease (Q37666293) (← links)
- Epidermolysis bullosa in France: management in the National Reference Center for Genodermatosis (Q37743906) (← links)
- Neonatal erythroderma (Q37771229) (← links)
- Cutaneous B-cell lymphoblastic lymphoma in children: A rare diagnosis (Q37950002) (← links)
- Congenital Erosive and Vesicular Dermatosis: A New Case and Review of the Literature (Q37972637) (← links)
- Insight into IKBKG/NEMO locus: report of new mutations and complex genomic rearrangements leading to incontinentia pigmenti disease (Q38171457) (← links)
- A new TRPV3 missense mutation in a patient with Olmsted syndrome and erythromelalgia (Q38180949) (← links)
- Haemangioma family burden: creation of a specific questionnaire (Q38199988) (← links)
- Infantile myofibromatosis: a series of 28 cases (Q38217413) (← links)
- Presence of chimeric maternally derived keratinocytes in cutaneous inflammatory diseases of children: the example of pityriasis lichenoides. (Q38439673) (← links)
- CEMARA an information system for rare diseases. (Q38505088) (← links)
- Combination of palmoplantar keratoderma and hair shaft anomalies, the warning signal of severe arrhythmogenic cardiomyopathy: a systematic review on genetic desmosomal diseases (Q38591830) (← links)
- Topical Corticosteroid Concerns Among Parents of Children with Psoriasis versus Atopic Dermatitis: A French Multicenter Cross-Sectional Study. (Q38604365) (← links)
- Skin Biopsy in Netherton Syndrome: A Histological Review of a Large Series and New Findings. (Q38716088) (← links)
- Interleukin-36-receptor antagonist deficiency and generalized pustular psoriasis (Q39217108) (← links)
- Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti (Q40312508) (← links)
- Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas. (Q42514400) (← links)
- Oral epigallocatechin-3-gallate for treatment of dystrophic epidermolysis bullosa: a multicentre, randomized, crossover, double-blind, placebo-controlled clinical trial. (Q42934969) (← links)
- Efficacy of propranolol in hepatic infantile hemangiomas with diffuse neonatal hemangiomatosis (Q43058150) (← links)
- Severe cutaneous papillomavirus disease after haemopoietic stem-cell transplantation in patients with severe combined immune deficiency caused by common gammac cytokine receptor subunit or JAK-3 deficiency (Q44243015) (← links)