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Nail dystrophy in focal acral hyperkeratosis: a distinctive feature?
- Published in:
- 2008
- By:
- Publication type:
- Letter
Familial palmoplantar keratoderma: not always hereditary.
- Published in:
- 2007
- By:
- Publication type:
- Letter
A systematic review of US state environmental legislation and regulation with regards to the prevention of neurodevelopmental disabilities and asthma.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Flüchtige Terpene in Pilzen.
- Published in:
- Archiv der Pharmazie, 1975, v. 308, n. 11, p. 843, doi. 10.1002/ardp.19753081108
- By:
- Publication type:
- Article
The nature of microemboli in patients with artificial heart valves.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Compound heterozygosity for mutations in the hairless gene causes atrichia with papular lesions.
- Published in:
- British Journal of Dermatology, 2003, v. 148, n. 3, p. 553, doi. 10.1046/j.1365-2133.2003.05177.x
- By:
- Publication type:
- Article
Sweat secretion, stratum corneum hydration, small nerve function and pruritus in patients with advanced chronic renal failure.
- Published in:
- British Journal of Dermatology, 1995, v. 133, n. 4, p. 561, doi. 10.1111/j.1365-2133.1995.tb02705.x
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- Publication type:
- Article
Enhancement of the production of fungal volatiles employing different adsorbents.
- Published in:
- Flavour & Fragrance Journal, 1989, v. 4, n. 2, p. 77, doi. 10.1002/ffj.2730040209
- By:
- Publication type:
- Article
Accumulation of africanols in liquid cultures of Leptographium lundbergii.
- Published in:
- Flavour & Fragrance Journal, 1987, v. 2, n. 4, p. 175, doi. 10.1002/ffj.2730020408
- By:
- Publication type:
- Article
Deleterious mutations in SPINK5 in a patient with congenital ichthyosiform erythroderma: molecular testing as a helpful diagnostic tool for Netherton syndrome.
- Published in:
- Clinical & Experimental Dermatology, 2004, v. 29, n. 5, p. 513, doi. 10.1111/j.1365-2230.2004.01589.x
- By:
- Publication type:
- Article
P3‐540: IMPLICATIONS OF SLEEP DISPARITIES FOR COGNITIVE TEST PERFORMANCE AMONG AFRICAN AMERICAN AND WHITE OLDER ADULTS: PRELIMINARY EVIDENCE FROM TWO WISCONSIN COHORTS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1178, doi. 10.1016/j.jalz.2019.06.3576
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- Publication type:
- Article
P1‐318: OBSTRUCTIVE SLEEP APNEA IS ASSOCIATED WITH LOWER MEMORY FUNCTION IN MIDDLE‐AGED ADULTS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P413, doi. 10.1016/j.jalz.2018.06.325
- By:
- Publication type:
- Article
O1‐03‐04: HYPOXIA DURING SLEEP IS ASSOCIATED WITH HIPPOCAMPAL VOLUME IN COGNITIVELY UNIMPAIRED ADULTS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P220, doi. 10.1016/j.jalz.2018.06.2345
- By:
- Publication type:
- Article
IC‐P‐150: HYPOXIA DURING SLEEP IS ASSOCIATED WITH HIPPOCAMPAL VOLUME IN COGNITIVELY UNIMPAIRED ADULTS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P128, doi. 10.1016/j.jalz.2018.06.2216
- By:
- Publication type:
- Article
IC‐P‐089: OBSTRUCTIVE SLEEP APNEA IS ASSOCIATED WITH LOWER MEMORY FUNCTION IN MIDDLE‐AGED ADULTS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P74, doi. 10.1016/j.jalz.2018.06.2153
- By:
- Publication type:
- Article
REGIONAL DEFICIT IN SLEEPING BRAIN ACTIVITY ASSOCIATED WITH TAU AND AMYLOID PATHOLOGY IN COGNITIVELY HEALTHY MIDDLE-AGED ADULTS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P41, doi. 10.1016/j.jalz.2017.06.2321
- By:
- Publication type:
- Article
REGIONAL DEFICIT IN SLEEPING BRAIN ACTIVITY ASSOCIATED WITH TAU AND AMYLOID PATHOLOGY IN COGNITIVELY HEALTHY MIDDLE-AGED ADULTS.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P1128, doi. 10.1016/j.jalz.2017.06.1640
- By:
- Publication type:
- Article
POOR SLEEP QUALITY IS ASSOCIATED WITH CSF MARKERS OF AMYLOID DEPOSITION IN COGNITIVELY HEALTHY ADULTS AT RISK FOR ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P561, doi. 10.1016/j.jalz.2016.06.1095
- By:
- Publication type:
- Article
A035: Sildenafil changes blood pressure profiles of hypertensive and normotensive impotent males.
- Published in:
- American Journal of Hypertension, 1999, v. 12, p. 155A, doi. 10.1016/S0895-7061(99)80557-3
- By:
- Publication type:
- Article
A034: Sildenafil effect on waking cardiovascular parameters in hypertensive impotent males.
- Published in:
- American Journal of Hypertension, 1999, v. 12, p. 155A, doi. 10.1016/S0895-7061(99)80556-1
- By:
- Publication type:
- Article
Potential relevance of low-intensity microembolic signals by TCD monitoring.
- Published in:
- Neurological Sciences, 2011, v. 32, n. 1, p. 107, doi. 10.1007/s10072-010-0429-8
- By:
- Publication type:
- Article
ST18 affects cell–cell adhesion in pemphigus vulgaris in a tumour necrosis factor‐α‐dependent fashion.
- Published in:
- British Journal of Dermatology, 2021, v. 184, n. 6, p. 1153, doi. 10.1111/bjd.19679
- By:
- Publication type:
- Article
Identification of a founder mutation in KRT14 associated with Naegeli–Franceschetti–Jadassohn syndrome.
- Published in:
- British Journal of Dermatology, 2020, v. 183, n. 4, p. 756, doi. 10.1111/bjd.19123
- By:
- Publication type:
- Article
Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility.
- Published in:
- British Journal of Dermatology, 2020, v. 183, n. 4, p. 614, doi. 10.1111/bjd.18921
- By:
- Publication type:
- Article
Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicin.
- Published in:
- British Journal of Dermatology, 2020, v. 183, n. 1, p. 114, doi. 10.1111/bjd.18718
- By:
- Publication type:
- Article
Treatment of epidermolysis bullosa pruriginosa‐associated pruritus with dupilumab.
- Published in:
- British Journal of Dermatology, 2020, v. 182, n. 6, p. 1495, doi. 10.1111/bjd.18855
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- Publication type:
- Article
肉毒杆菌毒素可帮助先天性厚甲症患者缓解足部症状.
- Published in:
- British Journal of Dermatology, 2020, v. 182, n. 3, p. e105, doi. 10.1111/bjd.18836
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- Publication type:
- Article
Botulinum toxin can help with foot symptoms in patients with pachyonychia congenita.
- Published in:
- British Journal of Dermatology, 2020, v. 182, n. 3, p. e92, doi. 10.1111/bjd.18823
- By:
- Publication type:
- Article
Revisiting pachyonychia congenita: a case‐cohort study of 815 patients.
- Published in:
- British Journal of Dermatology, 2020, v. 182, n. 3, p. 738, doi. 10.1111/bjd.18794
- By:
- Publication type:
- Article
Symptomatic mucosal involvement in pachyonychia congenita: challenges in infants and young children.
- Published in:
- British Journal of Dermatology, 2020, v. 182, n. 3, p. 708, doi. 10.1111/bjd.18742
- By:
- Publication type:
- Article
A treatment protocol for botulinum toxin injections in the treatment of pachyonychia congenita‐associated keratoderma.
- Published in:
- British Journal of Dermatology, 2020, v. 182, n. 3, p. 671, doi. 10.1111/bjd.18169
- By:
- Publication type:
- Article
Identification of a recurrent mutation in ATP2C1 demonstrates that papular acantholytic dyskeratosis and Hailey–Hailey disease are allelic disorders.
- Published in:
- British Journal of Dermatology, 2018, v. 179, n. 4, p. 1001, doi. 10.1111/bjd.16915
- By:
- Publication type:
- Article
Striate palmoplantar keratoderma resulting from a missense mutation in DSG1.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Chronic pain in pachyonychia congenita: evidence for neuropathic origin.
- Published in:
- British Journal of Dermatology, 2018, v. 179, n. 1, p. 154, doi. 10.1111/bjd.16217
- By:
- Publication type:
- Article
Punctate palmoplantar keratoderma: an unusual mutation causing an unusual phenotype.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
Novel <italic>POFUT1</italic> mutation associated with hidradenitis suppurativa–Dowling–Degos disease firm up a role for Notch signalling in the pathogenesis of this disorder: reply from the authors.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
由PSENEN始祖突变引起的结合了化脓性汗腺炎与道林‐德戈斯(Dowling–Degos)病的表现型
- Published in:
- British Journal of Dermatology, 2018, v. 178, n. 2, p. e177, doi. 10.1111/bjd.16303
- By:
- Publication type:
- Article
A phenotype combining hidradenitis suppurativa with Dowling–Degos disease caused by a founder mutation in <italic>PSENEN</italic>.
- Published in:
- British Journal of Dermatology, 2018, v. 178, n. 2, p. e160, doi. 10.1111/bjd.16285
- By:
- Publication type:
- Article
A phenotype combining hidradenitis suppurativa with Dowling–Degos disease caused by a founder mutation in <italic>PSENEN</italic>.
- Published in:
- British Journal of Dermatology, 2018, v. 178, n. 2, p. 502, doi. 10.1111/bjd.16000
- By:
- Publication type:
- Article
Rituximab and short-course prednisone as the new gold standard for new-onset pemphigus vulgaris and pemphigus foliaceus.
- Published in:
- 2017
- By:
- Publication type:
- Editorial
IgA pemphigus: lumping or splitting?
- Published in:
- British Journal of Dermatology, 2017, v. 177, n. 2, p. 581, doi. 10.1111/bjd.15627
- By:
- Publication type:
- Article
Image Gallery: Massive localized lymphoedema.
- Published in:
- British Journal of Dermatology, 2017, v. 176, n. 5, p. e95, doi. 10.1111/bjd.15370
- By:
- Publication type:
- Article
Report of the 13th Annual International Pachyonychia Congenita Consortium Symposium.
- Published in:
- British Journal of Dermatology, 2017, v. 176, n. 5, p. 1144, doi. 10.1111/bjd.15417
- By:
- Publication type:
- Article
Happle-Tinschert syndrome can be caused by a mosaic SMO mutation and is suggested to be a variant of Curry-Jones syndrome: reply from the authors.
- Published in:
- British Journal of Dermatology, 2016, v. 175, n. 5, p. 1109, doi. 10.1111/bjd.14979
- By:
- Publication type:
- Article
Pemphigoid: diversity in evolution.
- Published in:
- British Journal of Dermatology, 2016, v. 175, n. 4, p. 676, doi. 10.1111/bjd.14827
- By:
- Publication type:
- Article
Segmental basal cell naevus syndrome caused by an activating mutation in smoothened.
- Published in:
- British Journal of Dermatology, 2016, v. 175, n. 1, p. 178, doi. 10.1111/bjd.14425
- By:
- Publication type:
- Article
BJD in translation.
- Published in:
- 2015
- By:
- Publication type:
- Editorial
Paraneoplastic pemphigus: an entity still in search of an identity?
- Published in:
- British Journal of Dermatology, 2015, v. 173, n. 6, p. 1363, doi. 10.1111/bjd.14277
- By:
- Publication type:
- Article
Extensive lentigo simplex, linear epidermolytic naevus and epidermolytic naevus comedonicus caused by a somatic mutation in KRT10.
- Published in:
- British Journal of Dermatology, 2015, v. 173, n. 1, p. 293, doi. 10.1111/bjd.13616
- By:
- Publication type:
- Article
Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes.
- Published in:
- British Journal of Dermatology, 2014, v. 171, n. 6, p. 1521, doi. 10.1111/bjd.13176
- By:
- Publication type:
- Article