Results 261 to 270 of about 1,787,415 (342)

Nitrate Prevents Sjögren's Disease by Modulating T Helper Cells via NF‐κB Pathway Suppression

Oral Diseases, EarlyView.
ABSTRACT Objective Sjögren's disease (SjD) is a chronic autoimmune disease characterized by abnormal T helper (Th) cell distribution in the salivary glands (SGs). Although nitrate can regulate immune responses and preserve SGs function, its preventive effects on SjD remain unexplored.
Conglin Du, Zi Yang, Yang Yang, Chunmei Zhang, Hideaki Kagami, Xianqi Li, Liang Hu, Junji Xu, Jian Zhou   +8 more
wiley   +1 more source

Challenging differentiation of oral malignant lymphoma from osteomyelitis of the jawbone: A case report. [PDF]

Mol Clin Oncol
Munekata T, Asaka T, Sakata KI, Kimura T, Matsuda A, Maishi N, Satoh C, Kitagawa Y.   +7 more
europepmc   +1 more source

Effect of Periodontal Treatment on Metabolic Syndrome Parameters: A Systematic Review

Oral Diseases, EarlyView.
ABSTRACT Aim To evaluate the effects of periodontal treatment on metabolic syndrome (MS) parameters and systemic inflammatory biomarker levels in patients affected by both MS and periodontitis. Methods A systematic search was conducted to identify randomized controlled trials (RCTs) with a follow‐up ≥ 1 month comparing a more intense periodontal ...
Anna Simonelli, Filippo Citterio, Fabio Falcone, Francesco D'Aiuto, Nicola Marco Sforza, Salvatore Corrao, Giorgio Sesti, Leonardo Trombelli   +7 more
wiley   +1 more source

Psychiatric‐onset neuronal intranuclear inclusion disease in a psychiatry‐based dementia‐enriched cohort in Japan

Psychiatry and Clinical Neurosciences, EarlyView.
Aim A GGC repeat expansion in the 5′ untranslated region of NOTCH2NLC is a genetic cause of Neuronal Intranuclear Inclusion Disease (NIID) that exhibits cognitive, motor, and autonomic dysfunction. Our objective is to determine whether there are undiagnosed NIID cases in a psychiatry‐based dementia‐enriched cohort and to identify their clinical ...
Tesshin Miyamoto, Kohji Mori, Shoshin Akamine, Shizuko Kondo, Shiho Gotoh, Ryota Uozumi, Sumiyo Umeda, Hanako Koguchi‐Yoshioka, Satoshi Nojima, Daiki Taomoto, Yuto Satake, Takashi Suehiro, Hideki Kanemoto, Kenji Yoshiyama, Takashi Morihara, Manabu Ikeda   +15 more
wiley   +1 more source

Heterozygous DSP in‐frame deletion in a poodle with syndromic ichthyosis involving additional hair and tooth abnormalities

Sarah Kiener, Georg Lehner, Vidhya Jagannathan, Monika Welle, Tosso Leeb   +4 more
openalex   +1 more source

Peeling Skin, Leukonychia, Acral Punctate Keratoses, Cheilitis and Knuckle Pads (PLACK) Syndrome: An Updated Review of Cases and Identification of a Recurrent CAST Variant in Two Patients

Pediatric Dermatology, EarlyView.
ABSTRACT Peeling skin, leukonychia, acral punctate keratoses, cheilitis, and knuckle pads (PLACK) syndrome (OMIM616295) is an exceptionally rare autosomal recessive genodermatosis caused by loss‐of‐function pathogenic variants in the CAST gene, encoding calpastatin.
Fiona Haxho, Richard M. Haber, Janan Mohamad, Ofer Sarig, Eli Sprecher, Renée Perrier, Dana Boctor, Michele Ramien   +7 more
wiley   +1 more source

Mediating factors associated with alcohol intake and periodontal condition. [PDF]

Front Oral Health
Kusu Y, Furuta M, Kageyama S, Yamashita Y, Takeshita T.   +4 more
europepmc   +1 more source

Orthodontics in Pediatric Osteoporosis: A Narrative Literature Review. [PDF]

Children (Basel)
Gravia AP, Vastardis H, Tsolakis AI, Doulgeraki A.   +3 more
europepmc   +1 more source

GPR56/ADGRG1 regulates development and maintenance of peripheral myelin [PDF]

, 2018
Ackerman, Sarah D, D\u27Rozario, Mitchell, et al,, Gamble, Paul, Harty, Breanne L, MacEwan, Matthew R, Mogha, Amit, Monk, Kelly R, Ray, Wilson Zachary, Sanchez, Nicholas E   +9 more
core   +1 more source

Charcot-Marie-Tooth Disease Type 1A Diagnosed Based on Abnormalities in a Nerve Conduction Study in a Patient with Myotonic Dystrophy Type 1: A Case Report

, 2018
Hyung Nam Lee, Yu Hui Won
openalex   +1 more source