26 results on '"Di Leo E."'
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2. Variable phenotypic expression of homozygous familial hypobetalipoproteinaemia due to novel APOB gene mutations.
3. Focus on the agents most frequently responsible for perioperative anaphylaxis.
4. Diagnosis of Latex Allergy: The Importance of Hev b 11.
5. 590 IN VITRO FUNCTIONAL CHARACTERIZATION OF NOVEL AMINO ACID SUBSTITUTIONS IN PCSK9 FOUND IN HYPOCHOLESTEROLEMIC SUBJECTS
6. Immediate rhinoconjunctivitis induced by metamizole: an allergic reaction?
7. Treatment of acquired cold urticaria with rupatadine.
8. Fixed drug eruption due to sodium fluorescein.
9. Is black henna responsible for asthma and cross reactivity with latex?
10. Mo-W5:3 Molecular diagnosis and treatment of hypobetalipoproteinemia
11. 608 HYPOALPHA-HYPOBETALIPOPROTEINEMIA (FAMILIAL COMBINED HYPOLIPIDEMIA) CAUSED BY LOSS OF FUNCTION MUTATIONS OF ANGPTL3 GENE
12. Maculopapular rash due to fluconazole.
13. Eyedrop-Induced Allergy: Clinical Evaluation and Diagnostic Protocol.
14. Dupilumab in atopic dermatitis: predictors of treatment outcome and time to response.
15. Long‐term effectiveness of dupilumab up to 52 weeks in atopic dermatitis in 253 adult patients.
16. Focus on the role of substance P in chronic urticaria.
17. WO15-OR-4 A NOVEL LOSS OF FUNCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL
18. W14.392 Familial hypobetalipoproteinemia with no truncated forms of apolipoprotein B detectable in plasma
19. Familial hypobetalipoproteinemia: Analysis of three Spanish cases with two new mutations in the APOB gene.
20. Kounis Syndrome induced by intravenous administration of piperacillin/tazobactam: A case report
21. Sensitization, asthma and allergic disease in young soccer players.
22. T04-P-042 Abnormal apo-B messenger RNA splicingin familial hypobetalipoproteinemia
23. 351 Familial hypolipoproteinemia in steatosic patients
24. Contact allergy to benzocaine in a condom.
25. Cutaneous adverse drug reactions to Fluticasone propionate and Deflazacort in an asthmatic patient.
26. 594 NOVEL MUTATIONS IN SAR1B AND MTP GENES IN CHYLOMICRON RETENTION DISEASE AND ABETALIPOPROTEINEMIA
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