Results 271 to 280 of about 573,345 (369)
<i>Rickettsia rickettsii</i> inactivated whole cell antigen vaccine protects against Rocky Mountain spotted fever independent of the adjuvant used. [PDF]
Latré de Laté P +12 more
europepmc +1 more source
Mortality in Serologically Unconfirmed Mediterranean Spotted Fever [with Reply]
Pablo Yagupsky +4 more
openalex +1 more source
Delayed Diagnosis of Sézary Syndrome: Lessons From a Psoriasiform Presentation
ABSTRACT Pruritic erythroderma is not always psoriasis. Resistant cases require a broad evaluation for cutaneous lymphoma. Early, timely diagnosis prevents disease progression, improves outcomes, and enhances quality of life, highlighting the need for re‐evaluation when conventional treatments fail.
Sudhan Neupane +3 more
wiley +1 more source
Spotted Fever Group Rickettsiae from Ticks Captured in Sudan
Çhiharu Morita +9 more
openalex +2 more sources
Polynesian pigs were brought to the Hawaiian Islands with Polynesian settlement in the mid‐1200s and represent part of the cultural legacy of Hawai‘i. Yet, the introduction of European pigs since 1778 and onward has put into question the ancestral composition of contemporary animals, and conservation efforts have been challenged by tension between the ...
Anna M. Mangan +8 more
wiley +1 more source
Rocky Mountain Spotted Fever in Mexico: A Call to Action. [PDF]
Álvarez-Hernández G +30 more
europepmc +1 more source
Abstract Mid‐trimester pregnancy loss (MTL), defined as a pregnancy loss occurring between 14 + 0 and 21 + 6 weeks of gestation, causes significant physical and emotional distress to women and presents clinical challenges to healthcare professionals. It is acknowledged that in low‐resource settings, this guideline might be applicable to births up to 28
Caroline E. Fox +46 more
wiley +1 more source
Epidemiology and clinical characteristics of Mediterranean spotted fever suspects in a university hospital, Tunisia, 2000-2020. [PDF]
Lamloumi M +7 more
europepmc +1 more source
ABSTRACT Phenylketonuria (PKU) is an autosomal recessive disorder caused by a deficiency of phenylalanine hydroxylase (PAH), leading to the accumulation of phenylalanine (Phe) and an increased risk of developmental disorders. Treatment involves a Phe‐restricted diet, amino acid supplements, and for a subset of patients, a tetrahydrobiopterin (BH4 ...
Per Lundkvist +3 more
wiley +1 more source

