The authors respond to the points raised in the Letters to the Editor raised by Ogden and Du Clos and by Foster. Ad 1: The debate of the classification of respirable cyrstalline silica is outside the scope of the technical paper. Ad 2: A standard for the determination of SWeRF is under development, in which indeed the provision is made that for a correct determination all quartz within the fine fraction needs to be liberated. Ad 3: Dustiness tests provide useful information for occupational hygienists, but are not suitable for fulfilling classification and labelling requirements. Ad 4: Pipette effects are not discussed in the paper because the difference between calculating the SWeRF from the particle size distribution and the SWeRF from sedimentation is very small.
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http://dx.doi.org/10.1093/annhyg/meu041 | DOI Listing |
Int J Womens Dermatol
March 2025
The Ronald O. Perelman Department of Dermatology, New York University Grossman School of Medicine, New York City, New York.
Objective: This review aims to consolidate available evidence, identify research gaps, and advocate for a more informed approach to the management of pityriasis rosea in pregnant individuals.
Data Sources: PubMed, Web of Science, and Directory of Open Access Journals were systematically searched based on the keywords "pityriasis rosea," "pityriasis circinate," "roseola annulate," "herpes tonsurans maculosus," "herald patch," and "pregnancy" on January 25, 2024 for publications between 1950 to 2024.
Study Selection: Studies containing outcomes data for pregnant patients with established PR were included.
Cureus
December 2024
Research and Development, Glenmark Pharmaceuticals Limited, Mumbai, IND.
Background Cough in common cold is often associated with rhinorrhoea and nasal congestion, requiring treatment with a cough suppressant, decongestant, and antihistamine. Bilastine is a non-sedating antihistamine, a preferred option over sedating antihistamines. A combination of bilastine, dextromethorphan, and phenylephrine is expected to provide non-sedating treatment for cough associated with a common cold or allergy.
View Article and Find Full Text PDFTarget Oncol
January 2025
Division of Hematology and SCT, Georgia Cancer Centre, Augusta, GA, USA.
Bosutinib is a second-generation tyrosine kinase inhibitor (TKI) approved for use in patients with newly diagnosed Philadelphia chromosome (Ph)-positive chronic phase (CP) chronic myeloid leukemia (CML), as well as Ph-positive CP, accelerated phase, or blast phase (with chemotherapy) CML resistant or intolerant to prior therapy. Clinical trials have shown bosutinib is effective as first-line therapy for patients with CML as well as in later lines of therapy after prior TKI failure. Bosutinib has an established safety profile; however, as with all TKIs approved for the treatment of CML, there are adverse events (AEs) that require management.
View Article and Find Full Text PDFIndian J Gastroenterol
January 2025
Institute of Translational Research, Asian Healthcare Foundation, Gachibowli, Hyderabad, 500 032, India.
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