Results 51 to 60 of about 733,986 (259)

Evolving Patterns in Inpatient Pediatric Consultations to Allergy/Immunology at an Academic Medical Center

International Journal of Medical Students
Background: Consultations to pediatric allergy/immunology are of benefit to many hospitalized inpatients, but there is limited current information about how T-cell receptor excision circles (TREC) screening may have changed these patterns for pediatric ...
Madeline Wurst, Anna Brameli, Matthew Krantz, R. Stokes Peebles, Jr., Yasmin Khan, Cosby A. Stone, Jr.   +5 more
doaj   +1 more source

Neurovascular Contacts in the Pathophysiology of Neuralgic Amyotrophy: An Observational Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Neuralgic amyotrophy (NA) is a prevalent, monophasic, multifocal immune‐mediated neuropathy. A distinctive characteristic of the disease is the occurrence of nerve or fascicle constrictions and torsions (NA‐associated focal nerve lesions, NAFL). The pathophysiology underlying this phenomenon remains to be fully elucidated.
Johannes Fabian Holle, Andreas Leha, Volker Limmroth, Wolfram Windisch, Maximilian Zimmermann   +4 more
wiley   +1 more source

Long‐Term Efficacy of Immunotherapy in Autoimmune Autonomic Ganglionopathy—A 10‐Year Follow Up Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Autoimmune autonomic ganglionopathy (AAG) is a rare but potentially treatable cause of severe autonomic failure. Evidence guiding long‐term immunotherapy, treatment sequencing, and residual autonomic impairment is limited. We evaluated long‐term treatment response, residual autonomic dysfunction, and relapse patterns in patients with
Giacomo Chiaro, Shiwen Koay, Gordon T. Ingle, Patricia McNamara, Laura Watson, Fion Bremner, Valeria Iodice   +6 more
wiley   +1 more source

Biochemical and clinical characteristics of creatine deficiency syndromes. [PDF]

, 2004
Creatine deficiency syndromes are a newly described group of inborn errors of creatine synthesis (arginine:glycine amidinotransferase (AGAT) deficiency and guanidinoacetate methyltransferase (GAMT) deficiency) and of creatine transport (creatine ...
Sykut-Cegielska, Jolanta, Stöckler-Ipsiroglu, Sylvia, Mercimek-Mahmutoglu, Saadet, Gradowska, Wanda   +3 more
core  

Virologic, immunologic, and clinical response to highly active antiretroviral therapy: the gender issue revisited

, 2003
Not the final published versionBACKGROUND: Highly active antiretroviral therapy (HAART) has dramatically improved the prognosis for patients with HIV. There is ongoing debate over a potential gender effect on patient outcome after HAART.
Phillips, AN, Johnson, A. M., Lungren, J. D., Moore, AL, Johnson, Anne M., Blaxhult, Anders, Katlama, Christine, Kirk, O., Lungren, Jens D., Dietrich, M., Blaxhult, A,, Blaxhult, A., Kirk, O, Blaxhult, A, Dietrich, M, Colebunders, Robert, Moore, A. L., Chiesi, A, Lundgren, Jens Dilling, Johnson, AM, Colebunders, R., Chiesi, Antonio, Lungren, JD, Katlama, C, Phillips, A. N., Dietrich, Manfred, Chiesi, A., Colebunders, R, Moore, Antonia L., Phillips, Andrew N., Katlama, C., Kirk, Ole   +31 more
core   +1 more source

Electroencephalographic Normalization as a Biomarker of Clinical Recovery in Down Syndrome Regression Disorder

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Down syndrome regression disorder is a syndrome characterized by subacute loss of cognitive, behavioral, and functional abilities in individuals with Down syndrome. Electroencephalography abnormalities are frequently observed during evaluation, but it remains unclear whether these findings represent a dynamic marker of disease ...
Jonathan D. Santoro, Mackenzie Silverman, Maeve C. Lucas, Mariam M. Yousuf, Samuel T. Otey, Stella V. Gray, Brittany Jordan, Madeline D. Kahan, Latanya D. Agurs, Michelle Van Hirtum Das, Deborah Holder, Devin King, Eileen A. Quinn, Ryan Kammeyer, Michael S. Rafii   +14 more
wiley   +1 more source

Family Study of Pediatric Patients with Primary Antibody Deficiencies

Iranian Journal of Allergy, Asthma and Immunology, 2013
Common variable immunodeficiency (CVID) and selective IgA deficiency (SIGAD) are the most common primary antibody deficiencies. These two diseases may have coincidence in one family and SIGAD can progress to CVID which suggest common underlying genetic ...
Nima Rezaei, Hassan Abolhassani, Amir Kasraian, Payam Mohammadinejad, Bamdad Sadeghi, Asghar Aghamohammadi   +5 more
doaj  

Clinical and Modifiable Factors Associated With Disability and Relapse in MOGAD: A Multicentre Cohort Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Factors associated with relapse course and disability in myelin oligodendrocyte glycoprotein antibody‐associated disease (MOGAD) remain incompletely understood. Objectives To identify clinical and modifiable factors associated with relapse and disability in MOGAD. Methods In this ambispective multicentre cohort study using data from
Yingtao Wang, Shaoxin Tao, Qiujia Wang, Xiaoyu Xu, Hui Yao, Zheng Liu, Dawei Li, Zhandong Qiu, Jinming Han, Jiangwei Xia, Qi Wang, Jun Sun, Kai Shao, Jiao Li, Shishuang Ruan, Yi Zhong, Jun Guo, Shougang Guo, Yue Huang, Guoliang Chai, Tao Jin, Hongyu Zhou, Junwei Hao, Yinan Zhao   +23 more
wiley   +1 more source

Primary antibody deficiency syndromes

, 2018
Primary antibody deficiency syndromes (PAD) are a group of primary immunodeficiencies (PID) characterized by reduced production of immunoglobulins and recurrent respiratory tract infections.
Larsen, Carsten Schade, Katzenstein, Terese L   +1 more
core   +1 more source

Evaluation of Humoral Immune Function in Patients with Chronic Idiopathic Thrombocytopenic Purpura

Iranian Journal of Allergy, Asthma and Immunology, 2013
Coincidence of autoimmune diseases such as immune thrombocytopenic purpura (ITP) with  immunodeficiencies has  been  reported  previously in  patients  who  suffered  from primary antibody deficiency (PAD). But there is no original study on immunological
Mohammad Saeid Rahiminejad, Mehrdad Mirmohammad Sadeghi, Payam Mohammadinejad, Bamdad Sadeghi, Hassan Abolhassani, Mohammad Mehdi Dehghani Firoozabadi, Seyed Mohammad Fathi, Hamid Rezvani, Gholamreza Bahoush, Mohammad Ali Ehsani, Mohammad Faranoush, Azim Mehrvar, Babak Torabi Sagvand, Mojtaba Ghadiani, Nima Rezaei, Asghar Aghamohammadi   +15 more
doaj