Results 111 to 120 of about 266,825 (311)

DePerio: Deep Learning‐Based Oral Inflammatory Load Quantification for Periodontal Applications

Advanced Intelligent Systems, EarlyView.
a) Inflammation and oral polymorphonuclear neutrophil (oPMN) Migration: Dental plaque accumulation leads to inflammation, prompting white blood cells (WBCs), particularly oPMNs, to migrate from blood vessels through the gingival epithelium into the oral cavity.
Fatemeh Soheili, Negin Masoudifar, Shahin Ebrahimi, Navid Mohaghegh, Mahdi S. M. H. Daneshvar, Mahdi Amrollahi Biouki, Yasaman Tahernezhad, Chunxiang Sun, Michael Glogauer, Ebrahim Ghafar‐Zadeh   +9 more
wiley   +1 more source

Radioactive Calcium Kinetics during High Calcium Intake in Osteoporosis* [PDF]

, 1965
Ernest Schwartz, Vincent A. Panariello, John Saeli   +2 more
openalex   +1 more source

Width of Clavicular Cortex in Osteoporosis [PDF]

, 1969
H. C. Anton
openalex   +1 more source

Further Evidence That Chondrocalcinosis 1 (CCAL1) is a Confirmed Mendelian Phenotype With a Known Molecular Basis

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Chondrocalcinosis (CCAL), also known as calcium pyrophosphate dihydrate deposition disease (CPPDD), is a frequent multifactorial condition in the elderly, but there are two rare autosomal dominant Mendelian forms, CCAL1 (OMIM %600668) and CCAL2. Only three families with molecularly proven CCAL1 have been reported.
Anna‐Christina Pansa, Mareike Selig, Markus Wingendorf, Matthew A. Brown, Oliver Bartsch   +4 more
wiley   +1 more source

Calcium Balance and Calcium Requirement in Spinal Osteoporosis

, 1962
B. E. C. Nordin
openalex   +1 more source

Osteoporosis [PDF]

, 1965
H. A. Sissons
openalex   +1 more source

De Novo Heterozygous ZFX Frameshift Variant in a Female With an X‐Linked Neurodevelopmental Disorder

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Germline ZFX variants are associated with an X‐linked neurodevelopmental disorder, with 14 males and 16 females reported to date. We describe a 20‐year‐old female with a heterozygous ZFX frameshift variant, p.(Met666Valfs*2), identified by genome sequencing, previously reported in an affected male.
Iftekhar A. Showpnil, Allison Daley, Emily R. Sites, Shayne M. Plourde, Jesse M. Hunter, Dennis W. Bartholomew, April N. Lehman, Daniel C. Koboldt, Rolf W. Stottmann   +8 more
wiley   +1 more source

An Introduction to the Study of Osteoporosis (Biochemical and Biophysical Research in Bone Ageing)

, 1962
C Casuccio
openalex   +1 more source

Early Detection of Osteoporosis by Dual Energy X-ray Absorptiometry [PDF]

, 1969
Asadullah Makhdoom, Muhammad Qasim Rahopoto, Khaleeque Ahmed Siddiqui, Ghulam Ali Qureshi   +3 more
openalex   +1 more source

Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Rare diseases impact approximately 1 in 10 people worldwide, and yet, less than 5% of all rare diseases currently have an approved treatment option available. This is due to many challenges unique to rare diseases, including small, diverse patient populations, the cost of drug development that is not proportionate to the number of patients who
Caleb P. Bupp, Elizabeth A. VanSickle, Julianne Michael, Chad R. Schultz, Kelly Nguyen, Melissa Hoefer, Surender Rajasekaran, André S. Bachmann   +7 more
wiley   +1 more source