Found: 11
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Pitted keratolysis: clinical manifestations in 53 cases.
- Published in:
- British Journal of Dermatology, 1997, v. 137, n. 2, p. 282, doi. 10.1046/j.1365-2133.1997.18211899.x
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- Publication type:
- Article
Identification of programmed cell death in normal human skin tissues by using specific labelling of fragmented DNA.
- Published in:
- British Journal of Dermatology, 1994, v. 131, n. 4, p. 521
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- Publication type:
- Article
Population pharmacokinetics of darbepoetin alpha in peritoneal dialysis and non-dialysis patients with chronic kidney disease after single subcutaneous administration.
- Published in:
- 2009
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- Publication type:
- Journal Article
Population pharmacokinetic modeling and model validation of a spicamycin derivative, KRN5500, in phase 1 study.
- Published in:
- 2001
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- Publication type:
- journal article
Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis with a homozygous deletion mutation in SDR9C7.
- Published in:
- British Journal of Dermatology, 2017, v. 177, n. 3, p. e62, doi. 10.1111/bjd.15315
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- Publication type:
- Article
Dowling-Degos disease with mutations in POFUT1 is clinicopathologically distinct from reticulate acropigmentation of Kitamura.
- Published in:
- British Journal of Dermatology, 2015, v. 173, n. 2, p. 584, doi. 10.1111/bjd.13702
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- Publication type:
- Article
Population pharmacokinetics of intravenous busulfan in patients undergoing hematopoietic stem cell transplantation.
- Published in:
- Bone Marrow Transplantation, 2006, v. 37, n. 4, p. 345, doi. 10.1038/sj.bmt.1705252
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- Publication type:
- Article
Herpes zoster of the nipple: rapid DNA-based diagnosis by the loop-mediated isothermal amplification method.
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- International Journal of STD & AIDS, 2010, v. 21, n. 1, p. 66, doi. 10.1258/ijsa.2009.009178
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- Publication type:
- Article
Mutations in SAM syndrome and palmoplantar keratoderma patients suggest genotype/phenotype correlations in DSG1 mutations.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2022, v. 36, n. 3, p. e215, doi. 10.1111/jdv.17752
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- Publication type:
- Article
Infant bald patch: ultrasonographic diagnosis of aplasia cutis congenita.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2017, v. 31, n. 6, p. e276, doi. 10.1111/jdv.14018
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- Publication type:
- Article
Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood.
- Published in:
- Journal of the European Academy of Dermatology & Venereology, 2013, v. 27, n. 9, p. 1182, doi. 10.1111/j.1468-3083.2012.04526.x
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- Publication type:
- Article