Results 171 to 180 of about 109,515 (359)

The Effect of Ear Acupuncture in Reducing Body Weight in Obesity Patients: A Meta-Analysis

, 2021
Utami Pangestu, Yulia Lanti Retno Dewi, Hanung Prasetya   +2 more
openalex   +2 more sources

The Critical Role of Fractionated Urine Glycosaminoglycans in the Evaluation of Mucopolysaccharidosis Type II in Four Unrelated Families

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Since 2015, Ann and Robert H. Lurie Children's Hospital has performed diagnostic testing for infants who screen positive for mucopolysaccharidosis type II (MPS II) on the Illinois newborn screen. Preliminary diagnostic testing includes measurement of plasma iduronate‐2‐sulfatase enzyme activity and urinary glycosaminoglycan analysis, followed ...
Carly A. Rasmussen, Monika Izdebski, Allison Paltzer, Rachel Hickey, Laura Pollard, Joshua Baker   +5 more
wiley   +1 more source

Approach to Atrial Pacing in an Extracardiac Fontan Patient: Avoiding Trans-Baffle Puncture Through Electroanatomical Mapping. [PDF]

JACC Clin Electrophysiol
Joshee SR, Rayfield C, Yeshwant S, Beaser A, Ozcan C, Schoenbeck G, Arora R, Zimmerman F, Earing M, Upadhyay GA.   +9 more
europepmc   +1 more source

Effect of Secondary Cold Reduction Rates on Microstructure, Texture and Earing Behavior of Double Reduction Tinplate. [PDF]

Materials (Basel), 2021
Tian P, Liao L, Zhu G, Kang Y.
europepmc   +1 more source

Nuclear and extended infrared emission in paired and isolated galaxies [PDF]

The empirical connection between gravitational and collisional interactions among galaxies and enhanced activity has been well-documented. However, the physical mechanisms which are responsible for triggering the various forms of activity have not been ...
Cutri, Roc M.
core   +1 more source

Long‐Term Follow Up of Two Patients With Variants in the Cluster 1031‐1159 of TRRAP Gene: Expanding the Phenotype of Developmental Delay With or Without Dysmorphic Facies and Autism

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide, Vinicius Contrucci Dantas Segarra, Siulan Vendramini‐Pittoli, Henrique Regonaschi Serigatto, Luiza Virmond, Heloisa Marcelina da Cunha Palhares, Fernanda Jehee, Ana Cristina Victorino Krepischi, Carla Rosenberg, Carlos Henrique Paiva Grangeiro, Nancy Mizue Kokitsu‐Nakata   +10 more
wiley   +1 more source

Teen Presentation of Dyssynchronous Left Ventricular Cardiomyopathy Secondary to Wolff-Parkinson-White Syndrome and Right-Sided Septal Pathway. [PDF]

JACC Case Rep
Shah PV, Patel DA, Ganigara M, Earing MG.   +3 more
europepmc   +1 more source

The association between cardiac magnetic resonance-derived aortic stiffness parameters and aortic dilation in young adults with bicuspid aortic valve: With and without coarctation of aorta. [PDF]

Am Heart J Plus, 2022
Chongthammakun V, Pan AY, Earing MG, Damluji AA, Goot BH, Cava JR, Gerardin JF.   +6 more
europepmc   +1 more source

Apex Ear Bloodletting, Dietary Counseling and Psychotropic Medication in Patients with Anxiety Treated with Auricular Acupuncture - A Double Blind Study

, 2019
Huang Wei Ling, Alexander Bystritsky, Md, Sahib Phd, Khalsa, Md, Michael Phd, Phd Cameron, Jason Schiffman, Md, Mba Ma, Florence Thibaut, Huang Wei, Ling, Huang Wei, Ling, W Huang, W Huang, W Huang, Wei Huang, Ling, W Huang   +21 more
openalex   +1 more source

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli, Stefania Della Vecchia, Patrizia Bergonzini, Elisa Caramaschi, Elisabetta Spezia, Claudia Parenti, Simona Filomena Madeo, Laura Lucaccioni, Cavalleri Francesca, Marisa Pugliese, Federico Raviglione, Clara Colonna, Olga Calabrese, Ilaria Stanghellini, Maria Carmen Marongiu, Enrico Biagioni, Anna Rita Ferrari, Roberta Battini, Lorenzo Iughetti   +18 more
wiley   +1 more source