557 results on '"Hohl D"'
Search Results
2. The thermal triple-axis-spectrometer EIGER at the continuous spallation source SINQ
3. Cross-linked envelopes in nail plate in lamellar ichthyosis
4. 483 PTCH1 inactivation is sufficient to cause basaloid follicular hamartoma in pediatric Nevoid basal cell carcinoma syndrome
5. Photobiologie
6. Exacerbation of mycosis fungoides masquerading as psoriasis under cytokine-pathway blockers
7. PTCH1 inactivation is sufficient to cause basaloid follicular hamartoma in paediatric Nevoid basal cell carcinoma syndrome
8. Photobiologie
9. Unusual dermatological presentation and immune phenotype in SCID due to an IL7R mutation: the value of whole-exome sequencing and the potential benefit of newborn screening
10. Computational materials science from first principles
11. Density Functional Calculations - A Database for Parameterizing Interatomic Potentials
12. Density Functional Calculations with Simulated Annealing — New Perspectives for Molecular Calculations
13. Papillon‐Lefevre syndrome treated by acitretin: case report and cytokine profile
14. 168 ARP-T1-associated Bazex-Dupré-Christol Syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies
15. Eccrine naevus: Case report with dermoscopic findings
16. Ichthyosen: Pathophysiologische Modelle der epidermalen Differenzierung
17. Non-immediate drug hypersensitivity reactions secondary to intravitreal anti-vascular endothelial growth factors
18. Genomic profiling of late-onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome
19. New and recurrent AAGAB mutations in punctate palmoplantar keratoderma
20. Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris
21. Pathologie digitale pour le dermato [Digital pathology for the dermatologist]
22. Diaper dermatitis prevalence and severity : global perspective on the impact of caregiver behavior
23. Deep Learning Techniques Revolutionize E&P – Two practical applications
24. Identification of the first nonsense CDSN mutation with expression of a truncated protein causing peeling skin syndrome type B
25. Pitiriasis rubra pilaris
26. Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12–q13
27. Induction of p38, tumour necrosis factor-α and RANTES by mechanical stretching of keratinocytes expressing mutant keratin 10R156H
28. Genomic profiling of late‐onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome
29. Bilateral Alopecia in a Six-year-old Boy: A Quiz
30. Proton Quantum Effects in High Pressure Hydrogen
31. Incidence of bullous pemphigoid and pemphigus in Switzerland: a 2-year prospective study
32. Transglutaminase 1-deficient recessive lamellar ichthyosis associated with a LINE-1 insertion in Jack Russell terrier dogs
33. Papillon‐Lefevre syndrome treated by acitretin: case report and cytokine profile.
34. Simultaneous manifestation of variegate porphyria in monozygotic twins
35. Evaluation of the Euromelanoma skin cancer screening campaign: the Swiss experience
36. Novel and recurring ABCA12 mutations associated with harlequin ichthyosis: implications for prenatal diagnosis
37. Density functional theory and biomolecules: a study of glycine, alanine, and their oligopeptides
38. Altered distribution of keratinization markers in epidermolytic hyperkeratosis
39. Ab initio molecular dynamics — Applications to the molecular and solid state physics of phosphorus
40. Novel CYLD mutations Spiegler-Brooke Syndrome: Identification of Aspartic Acid 681 as Crucial Amino Acid for Enzymatic Function
41. Keratinocytes Express and Secrete Inflammasome Proteins and Active Interleukin-1
42. Expression and Properties of the Ten LY6/PLAUR Genes Encoded on Chromosome 8q24.3
43. Pseudoxanthoma elasticum: evaluation of diagnostic criteria based on molecular data
44. Confirmation of the Origin of NISCH Syndrome
45. Clinical variation in X-linked dominant chondrodysplasia punctata (X-linked dominant ichthyosis)
46. Loricrin immunoreactivity in human skin: localization to specific granules (L-granules) in acrosyringia
47. Novel mutation of connexin 31 causing erythrokeratoderma variabilis
48. Management of congenital ichthyoses : European guidelines of care, part two
49. Management of congenital ichthyoses : European guidelines of care, part one
50. Mutations in the Rod Domains of Keratins 1 and 10 in Epidermolytic Hyperkeratosis
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