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Military Medicine|March 29, 2018
Extremely Delayed Diagnosis of Type II Hereditary Angioedema: Case Report and Review of the LiteratureJeremy Berger, Michael P Carroll, Edward Champoux, et al.
Biochemistry and Molecular Biology International|April 8, 1998
A novel p53 mutation hotspot at codon 132 (AAG-->AGG) in human renal cancerR Dahiya, G Deng, C Selph, et al.
Clinical Endocrinology|December 8, 2015
Glucocorticoid therapy for adrenal insufficiency: nonadherence, concerns and dissatisfaction with informationS C E Chapman, S Llahana, P Carroll, et al.
Mechanisms of Development|July 27, 2001
Dynamic expression patterns of the new protocadherin families CNRs and Pcdh-gamma during mouse odontogenesis: comparison with reelin expressionR Heymann, S Kallenbach, S Alonso, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|August 14, 2001
Sorting nexin-14, a gene expressed in motoneurons trapped by an in vitro preselection methodP Carroll, Y Renoncourt, O Gayet, et al.
Annals of Ophthalmology|April 1, 1978
Congenital medial canthal tendon malpositionR P Carroll, R B Wilkins, S Fredricks, et al.
The American Journal of Pathology|December 1, 1992
Changes in frequency, morphology, and behavior of tumors induced in mice by a polyoma virus mutant with a specifically altered oncogeneR Freund, C J Dawe, J P Carroll, et al.
Genes, Chromosomes & Cancer|June 1, 1997
Frequent homozygous deletion of cyclin-dependent kinase inhibitor 2 (MTS1, p16) in superficial bladder cancer detected by fluorescence in situ hybridizationM Balázs, P Carroll, R Kerschmann, et al.
The European Respiratory Journal|June 26, 2021
Alpha-1 antitrypsin deficiency: clarifying the role of the putative protective thresholdAlessandro N Franciosi, Daniel Fraughen, Tomás P Carroll, et al.
Diagnostic Microbiology and Infectious Disease|February 17, 2009
Molecular analysis of diversity within the genus Pseudomonas in the lungs of cystic fibrosis patientsTrajko Spasenovski, Mary P Carroll, Matthew S Payne, et al.
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