Browse Items (11 total)
- Tags: Syndrome
Membranous glomerulonephritis: treatment response and outcome in children
Tags: 2009, childhood, chlorambucil, clinical course, cyclophosphamide, glomerular-filtration-rate, glomerulonephropathy, glomerulosclerosis, Imam A, Journal Article, Kapur G, Mattoo T K, Membranous, Membranous glomerulonephritis, methylprednisolone, nephropathy, nephrotic, Nephrotic syndrome, pediatric nephrology, Pediatrics, Syndrome, systemic lupus erythematosus, Urology & Nephrology, Valentini R P
Understanding Bile Acid Signaling in Diabetes: From Pathophysiology to Therapeutic Targets.
Tags: 2019, BILE acids, Bile Acids and Salts, Chiang John Y L, cholesterol 7-alpha-hydroxylase, Cytoplasmic and Nuclear, Department of Integrative Medical Sciences, Diabetes & Metabolism Journal, Endocrinology & Metabolism, Farnesoid X receptor, farnesoid-x-receptor, Fatty Liver, fatty liver-disease, Ferrell Jessica M, G protein coupled receptors, G-protein-coupled, Gastrointestinal Microbiome, growth-factor 19, gut microbiota, hepatic steatosis, improves insulin sensitivity, Liver disease, Metabolic, NEOMED College of Medicine, Non-alcoholic fatty, Non-alcoholic Fatty Liver Disease, nuclear, Receptor, Receptors, September 2019 Update, serum fgf21 levels, Syndrome
Human quadrupeds, primate quadrupedalism, and Uner Tan Syndrome.
Tags: *Primates, 2014, Adolph Karen E, Adult, Animals, Child, Cole Whitney G, Department of Anatomy & Neurobiology, Evolution, Female, Gait/*physiology, Humans, Infant, Male, Molecular, NEOMED College of Medicine, PloS one, Posture/physiology, Raichlen David A, Robinson Scott R, Shapiro Liza J, Syndrome, Walking/*physiology, Young Jesse W
An unusual dermatitis with annular lesions.
Tags: 2008, Atopic/*pathology, Biopsy, Cernik Christina, Child, Congenital/*pathology, Department of Internal Medicine, Dermatitis, Diagnosis, Differential, Hair/*abnormalities/*pathology, Humans, Ichthyosiform Erythroderma, Janik Matthew, Male, NEOMED College of Medicine, Pediatric dermatology, Psoriasis/pathology, Scalp/pathology, Syndrome, Trevino Julian
Precordial Catch Syndrome in Elite Swimmers With Asthma.
Tags: 2016, Adolescence, Adolescent, Asthma – Complications, Asthma/*complications, Chest Pain – Etiology, Chest Pain/*etiology, Emergency Service, Hayes Don Jr, Hospital, Humans, Male, Mansour Heidi M, Pediatric emergency care, Strawbridge Heather, Swimming, Syndrome, Thoracic Wall, Thorax, Younger Bradley R
Exploring the scope of post-intensive care syndrome therapy and care: engagement of non-critical care providers and survivors in a second stakeholders meeting.
Tags: *Health Status, *Intensive Care Units, 2014, Awareness, Bemis-Dougherty Anita, Bienvenu O Joseph, Black Gary, Brady Susan, Brodsky Martin B, Continuity of Patient Care/*organization & administration, Critical care medicine, Critical Illness/*psychology, Davidson Judy E, Department of Pharmaceutical Sciences, Department of Pharmacy Practice, Deutschman Cliff, Doepp Diana, Elliott Doug, Flatley Carl, Fosnight Sue, Gittler Michelle, Gomez Belkys Teresa, Harvey Maurene A, Health Education, Hopkins Ramona O, Humans, Hyzy Robert, Iwashyna Theodore J, Louis Deborah, Mandel Ruth, Maxwell Carol, Mental Health, Muldoon Sean R, Needham Dale M, NEOMED College of Pharmacy, Perme Christiane S, Reilly Cynthia, Robinson Marla R, Rubin Eileen, Schmidt David M, Schuller Jessica, Scruth Elizabeth, Siegal Eric, Spill Gayle R, Sprenger Sharon, Straumanis John P, Survivors/*psychology, Sutton Pat, Swoboda Sandy M, Syndrome, Twaddle Martha L, United States, Wagner Jason, Weinert Craig, Wunsch Hannah
Exome sequence identified a c.320A \textgreater G ALG13 variant in a female with infantile epileptic encephalopathy with normal glycosylation and random X inactivation: Review of the literature.
Tags: *Mutation, *X Chromosome Inactivation, 2017, ALG13, Bastaki Fatma, CDG Is, Child, Congenital disorder of glycosylation, Congenital Disorders of Glycosylation/diagnosis/*genetics, European journal of medical genetics, Exome, Female, Glycosylation, Hamici Sana, Heterozygote, Humans, Infant, Infantile/diagnosis/*genetics, Khalifa Mohamed, Mental Retardation, Missense, N-Acetylglucosaminyltransferases/*genetics, Post-Translational, Preschool, Protein Processing, Spasms, Syndrome, Transferrin/metabolism, X-inactivation, X-Linked/diagnosis/*genetics
Pathophysiology of empty nose syndrome.
Tags: 2015, Brain – Physiopathology, Brain/physiopathology, Computer Simulation, Dyspnea – Physiopathology, Dyspnea/physiopathology, Empty nose syndrome, Houser Steven M, Humans, Nasal Mucosa – Innervation, Nasal Mucosa/*innervation, Nasal Obstruction – Physiopathology, Nasal Obstruction/*physiopathology, nasal sensation, Neural Pathways – Physiopathology, Olfactory Pathways/physiopathology, Postoperative Complications – Physiopathology, Postoperative Complications/*physiopathology, Pulmonary Ventilation/*physiology, Respiratory Airflow – Physiology, Sensory Receptor Cells – Physiology, Sensory Receptor Cells/*physiology, Sozansky Jeanie, Syndrome, The Laryngoscope, Thermoreceptors – Physiopathology, Thermoreceptors/physiopathology, Tomography, Trigeminal Nerve – Physiopathology, Trigeminal Nerve/physiopathology, turbinate surgery, Turbinates – Physiopathology, Turbinates – Surgery, Turbinates/*physiopathology/*surgery, Wound Healing – Physiology, Wound Healing/*physiology, X-Ray Computed