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PubPharm (49)
1
A retrospective study on the liver toxicity of oral retinoids in Chanarin-Dorfman syndrome
enthalten in:
Journal of the European Academy of Dermatology and Venereology : JEADV
| 2023
von
Valette, C.
|
Jonca, N.
|
Fischer, J.
| +26
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2
Mosaic GJB2 mutation A88V leading to diffuse neonatal hyperkeratosis and porokeratotic hamartoma
enthalten in:
Journal of the European Academy of Dermatology and Venereology : JEADV
| 2023
von
Letertre, O.
|
Jullie, M.
|
Reboul, M.
| +6
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3
Benefits of the Dermocosmetic Mineral 89 Probiotic Fractions Adjunct to Topical Retinoids for Anti-Aging Benefits
in:
Clinical, Cosmetic and Investigational Dermatology
| 2023
von
Valpaços C
|
Leclerc-Mercier S
|
Lopes L
| +10
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4
Skin biopsy is helpful in the diagnosis of hereditary fibrosing POIKiloderma with tendon contractures, myopathy and pulmonary fibrosis, due to FAM111B mutation
enthalten in:
Journal of the European Academy of Dermatology and Venereology : JEADV
| 2022
von
Leclerc-Mercier, S.
|
Mercier, S.
|
Bellon, N.
| +5
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5
Skin biopsy is helpful in the diagnosis of hereditary fibrosing POIKiloderma with tendon contractures, myopathy and pulmonary fibrosis, due to FAM111B mutation
enthalten in:
Journal of the European Academy of Dermatology and Venereology
| 2022
von
Leclerc‐Mercier, S.
|
Mercier, S.
|
Bellon, N.
| +5
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6
Childhood epidermal necrolysis and erythema multiforme major : a multicentre French cohort study of 62 patients
enthalten in:
Journal of the European Academy of Dermatology and Venereology : JEADV
| 2021
von
Giraud-Kerleroux, L.
|
Bellon, N.
|
Welfringer-Morin, A.
| +17
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7
Management of albinism : French guidelines for diagnosis and care
enthalten in:
Journal of the European Academy of Dermatology and Venereology : JEADV
| 2021
von
Moreno-Artero, E.
|
Morice-Picard, F.
|
Bremond-Gignac, D.
| +9
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8
Gastrostomy for infants with severe epidermolysis bullosa simplex in neonatal intensive care
enthalten in:
Orphanet journal of rare diseases
| 2021
von
Marro, M.
|
De Smet, S.
|
Caldari, D.
| +3
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9
Gastrostomy for infants with severe epidermolysis bullosa simplex in neonatal intensive care
enthalten in:
Orphanet journal of rare diseases
| 2021
von
Marro, M.
|
De Smet, S.
|
Caldari, D.
| +3
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10
Genotypic and phenotypic analysis of 34 cases of inherited junctional epidermolysis bullosa caused by COL17A1 mutations
enthalten in:
The British journal of dermatology
| 2021
von
Hérissé, A.
|
Charlesworth, A.
|
Bellon, N.
| +6
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The British journal of dermatology
9
Journal of the European Academy of Dermatology ...
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Acta dermato-venereologica
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Clinical microbiology and infection : the offic...
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13
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Epidermolysis bullosa
2
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Proteinase Inhibitory Proteins, Secretory
2
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Serine Peptidase Inhibitor Kazal-Type 5
1
3-ketodihydrosphingosine reductase
1
9Y8NXQ24VQ
1
Alcohol Oxidoreductases
1
Antigens, Viral
1
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1
Cell Cycle Proteins
1
Codon, Nonsense
1
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1
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1
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1
EBP protein, human
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Erscheinungszeitraum
18
2020-
28
2010-2019
3
2000-2009
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10
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