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Oculocutaneous tyrosinemia: A case report with delayed diagnosis and excellent response to dietary modification.
- Published in:
- Indian Journal of Dermatology, Venereology & Leprology, 2015, v. 81, n. 3, p. 303, doi. 10.4103/0378-6323.152744
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- Publication type:
- Article
NIR spectroscopy for reaction monitoring and reaction mixture identification of cycloaliphatic epoxides.
- Published in:
- Journal of Polymer Research, 2022, v. 29, n. 5, p. 1, doi. 10.1007/s10965-022-03038-x
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- Publication type:
- Article
The Alopecia Areata Severity and Morbidity Index (ASAMI) Study: Results From a Global Expert Consensus Exercise on Determinants of Alopecia Areata Severity.
- Published in:
- JAMA Dermatology, 2024, v. 160, n. 3, p. 341, doi. 10.1001/jamadermatol.2023.5869
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- Publication type:
- Article
A Global eDelphi Exercise to Identify Core Domains and Domain Items for the Development of a Global Registry of Alopecia Areata Disease Severity and Treatment Safety (GRASS).
- Published in:
- 2021
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- Publication type:
- journal article
Insights Into the Biology of Persistent Chemotherapy-Induced Alopecia via Genomic Approaches-An Avenue to Clinical Translation?
- Published in:
- 2020
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- Publication type:
- Editorial
Odd-looking hair and progressive alopecia in mother and son.
- Published in:
- 2014
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- Publication type:
- journal article
Odd-Looking Hair and Progressive Alopecia in Mother and Son.
- Published in:
- JAMA Dermatology, 2014, v. 150, n. 5, p. 567, doi. 10.1001/jamadermatol.2013.8078
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- Publication type:
- Article
Genome-wide shRNA screen reveals increased mitochondrial dependence upon mTORC2 addiction.
- Published in:
- Oncogene, 2011, v. 30, n. 13, p. 1551, doi. 10.1038/onc.2010.539
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- Publication type:
- Article
MTHFR 677 TT genotype in a mother and her child with Down syndrome, atrioventricular canal and exstrophy of the bladder: implications of a mutual genetic risk factor?
- Published in:
- 2006
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- Publication type:
- journal article
LITHIUM MINERALS AND COMPOUNDS IN CERAMICS *.
- Published in:
- Journal of the American Ceramic Society, 1938, v. 21, n. 5, p. 189, doi. 10.1111/j.1151-2916.1938.tb15763.x
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- Publication type:
- Article
Supercollision cooling in undoped graphene.
- Published in:
- Nature Physics, 2013, v. 9, n. 2, p. 109, doi. 10.1038/nphys2494
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- Publication type:
- Article
Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 ( FCRL3) gene in alopecia areata.
- Published in:
- International Journal of Immunogenetics, 2006, v. 33, n. 6, p. 393, doi. 10.1111/j.1744-313X.2006.00633.x
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- Publication type:
- Article
Structural Damage Location with Fiber Bragg Grating Rosettes and Lamb Waves.
- Published in:
- Structural Health Monitoring, 2007, v. 6, n. 4, p. 299, doi. 10.1177/1475921707081974
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- Publication type:
- Article
Structural Monitoring Using Fiber-Optic Bragg Grating Sensors.
- Published in:
- Structural Health Monitoring, 2003, v. 2, n. 2, p. 145
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- Publication type:
- Article
Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypes.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 12, p. 3900, doi. 10.1002/ajmg.a.62438
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- Publication type:
- Article
Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes.
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 11, p. 2555, doi. 10.1002/ajmg.a.37233
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- Publication type:
- Article
Corrigendum: Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.
- Published in:
- 2009
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- Publication type:
- Correction Notice
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.
- Published in:
- Nature Genetics, 2009, v. 41, n. 2, p. 228, doi. 10.1038/ng.276
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- Publication type:
- Article
G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth.
- Published in:
- Nature Genetics, 2008, v. 40, n. 3, p. 329, doi. 10.1038/ng.84
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- Publication type:
- Article
Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin.
- Published in:
- Nature Genetics, 2003, v. 34, n. 2, p. 151, doi. 10.1038/ng1163
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- Publication type:
- Article
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease.
- Published in:
- Nature Genetics, 2001, v. 28, n. 3, p. 218, doi. 10.1038/90050
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- Publication type:
- Article
Detection of squamous cell carcinoma of the oral cavity by imaging 5-aminolevulinic acid-induced protoporphyrin IX fluorescence.
- Published in:
- 2000
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- Publication type:
- journal article
Curriculum „Trachealkanülenmanagement in der Dysphagietherapie".
- Published in:
- HNO, 2024, v. 72, n. 6, p. 393, doi. 10.1007/s00106-024-01454-7
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- Publication type:
- Article
Die Schädelbasischirurgie im deutschen DRG-System – Neue Zuordnung wichtiger Prozeduren.
- Published in:
- HNO, 2023, v. 71, n. 12, p. 811, doi. 10.1007/s00106-023-01380-0
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- Publication type:
- Article
Auswirkungen der SARS-CoV‑2-Pandemie auf die universitäre Hals-Nasen-Ohren-Heilkunde im Bereich der Forschung, Lehre und Weiterbildung.
- Published in:
- HNO, 2021, v. 69, n. 8, p. 633, doi. 10.1007/s00106-021-01001-8
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- Publication type:
- Article
Therapie der rezidivierten und fernmetastasierten Plattenepithelkarzinome des Kopf-Hals-Bereichs: Highlights des ASCO-Meetings 2019.
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- HNO, 2019, v. 67, n. 12, p. 898, doi. 10.1007/s00106-019-00773-4
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- Publication type:
- Article
Neue Aspekte in der Behandlung von Schilddrüsenkarzinomen: Highlights vom ASCO-Kongress 2019.
- Published in:
- HNO, 2019, v. 67, n. 12, p. 925, doi. 10.1007/s00106-019-00764-5
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- Publication type:
- Article
Narrow band imaging for early diagnosis of epithelial dysplasia and microinvasive tumors in the upper aerodigestive tract.
- Published in:
- HNO, 2017, v. 65, p. 5, doi. 10.1007/s00106-016-0284-x
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- Publication type:
- Article
Optische Diagnoseverfahren zur Verbesserung der Tumorfrühdiagnostik im oberen Luft-Speise-Weg.
- Published in:
- 2016
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- Publication type:
- Editorial
Optische Diagnoseverfahren zur Tumorfrühdiagnostik im oberen Luft-Speise-Weg.
- Published in:
- HNO, 2016, v. 64, n. 1, p. 41, doi. 10.1007/s00106-015-0104-8
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- Publication type:
- Article
'Narrow band imaging' zur Früherkennung epithelialer Dysplasien und mikroinvasiver Karzinome im oberen Luft-Speise-Weg.
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- HNO, 2016, v. 64, n. 1, p. 19, doi. 10.1007/s00106-015-0108-4
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- Publication type:
- Article
Nichtinvasive Bildgebung mittels Autofluoreszenzendoskopie.
- Published in:
- HNO, 2016, v. 64, n. 1, p. 13, doi. 10.1007/s00106-015-0095-5
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- Publication type:
- Article
Fluoreszenzbildgebung in der Laryngologie.
- Published in:
- HNO, 2016, v. 64, n. 1, p. 4, doi. 10.1007/s00106-015-0098-2
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- Publication type:
- Article
Optische Kohärenztomographie zur Früherkennung epithelialer Dysplasien und mikroinvasiver Karzinome im oberen Luft-Speise-Weg.
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- HNO, 2016, v. 64, n. 1, p. 34, doi. 10.1007/s00106-015-0102-x
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- Publication type:
- Article
Larynxpapillomatose.
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- HNO, 2008, v. 56, n. 12, p. 1190, doi. 10.1007/s00106-008-1711-4
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- Article
Wundheilungsstörung nach Tonsillektomie.
- Published in:
- HNO, 2008, v. 56, n. 7, p. 717, doi. 10.1007/s00106-007-1568-y
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- Publication type:
- Article
Das zervikale Hautemphysem.
- Published in:
- HNO, 2007, v. 55, n. 2, p. 121, doi. 10.1007/s00106-006-1389-4
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- Publication type:
- Article
Myxomatöse Neoplasien des Nasenseptums.
- Published in:
- HNO, 2007, v. 55, n. 1, p. 51, doi. 10.1007/s00106-005-1369-0
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- Publication type:
- Article
Uncombable hair improved by biotin.
- Published in:
- JEADV Clinical Practice, 2023, v. 2, n. 2, p. 313, doi. 10.1002/jvc2.105
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- Publication type:
- Article
Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2.
- Published in:
- Experimental Dermatology, 2017, v. 26, n. 6, p. 536, doi. 10.1111/exd.13123
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- Publication type:
- Article
Genetics and other factors in the aetiology of female pattern hair loss.
- Published in:
- Experimental Dermatology, 2017, v. 26, n. 6, p. 510, doi. 10.1111/exd.13373
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- Publication type:
- Article
Identification of an Alu-mediated 12.2-kb deletion of the complete LPAR6 ( P2 RY5) gene in a Turkish family with hypotrichosis and woolly hair.
- Published in:
- Experimental Dermatology, 2012, v. 21, n. 6, p. 469, doi. 10.1111/j.1600-0625.2012.01504.x
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- Publication type:
- Article
Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: No association with female pattern hair loss identified.
- Published in:
- Experimental Dermatology, 2012, v. 21, n. 5, p. 390, doi. 10.1111/j.1600-0625.2012.01469.x
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- Publication type:
- Article
A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31.
- Published in:
- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0129811
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- Publication type:
- Article
Recent Changes to the Community Reinvestment Act and Their Impact on Community Banks and Rural Economies.
- Published in:
- North Carolina School Banking Institute Journal, 2006, v. 10, p. 157
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- Publication type:
- Article
First East Asian case of uncombable hair syndrome.
- Published in:
- Journal der Deutschen Dermatologischen Gesellschaft, 2024, v. 22, n. 10, p. 1433, doi. 10.1111/ddg.15498
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- Publication type:
- Article
Erster ostasiatischer Fall des Syndroms der unkämmbaren Haare.
- Published in:
- Journal der Deutschen Dermatologischen Gesellschaft, 2024, v. 22, n. 10, p. 1433, doi. 10.1111/ddg.15498_g
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- Publication type:
- Article
Genexpressionsprofile beim Porokarzinom deuten auf heterogene Tumorentwicklung hin und untermauern Porome als Vorläuferläsionen.
- Published in:
- Journal der Deutschen Dermatologischen Gesellschaft, 2024, v. 22, n. 8, p. 1115, doi. 10.1111/ddg.15445_g
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- Publication type:
- Article
Gene expression profiling in porocarcinoma indicates heterogeneous tumor development and substantiates poromas as precursor lesions.
- Published in:
- Journal der Deutschen Dermatologischen Gesellschaft, 2024, v. 22, n. 8, p. 1115, doi. 10.1111/ddg.15445
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- Publication type:
- Article
POGLUT1‐Varianten bei Morbus Dowling‐Degos ‐ Assoziation mit spezifischen klinischen und histopathologischen Merkmalen?
- Published in:
- Journal der Deutschen Dermatologischen Gesellschaft, 2023, v. 21, n. 5, p. 540, doi. 10.1111/ddg.15111_g
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- Publication type:
- Article