Results 81 to 90 of about 1,512,505 (195)

Vitamin‐Responsive Disorders: From Molecular Basis to Clinical Presentation and Therapy

Journal of Inherited Metabolic Disease, Volume 49, Issue 4, July 2026.
ABSTRACT Vitamin‐dependent cofactors are essential for numerous metabolic reactions, and defects affecting their uptake, conversion, utilisation, or regeneration constitute a heterogeneous group of inherited metabolic disorders (IMDs). Although dietary vitamin intake is sufficient to sustain coenzyme synthesis in healthy individuals, it is insufficient
Cécile Acquaviva, Yann Nadjar, Manuel Schiff, Christine Vianey‐Saban, Alain Fouilhoux, Jean‐François Benoist   +5 more
wiley   +1 more source

Spectrum of acute flaccid paralysis in children [PDF]

, 2016
Acute flaccid paralysis (AFP) is a clinical syndrome characterized by rapid onset of weakness in a child aged less than 15 years due to any cause when polio is suspected(1).
Zia ur Rehman, M., Ali, Shaila, Sultan, Tipu   +2 more
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Bioinformatics‐Driven Design and Evaluation of Recombinant Multi‐Epitope Immunogens Derived From Snake Venom Toxins as Potential Antivenom Candidates

Proteins: Structure, Function, and Bioinformatics, Volume 94, Issue 7, Page 1403-1426, July 2026.
ABSTRACT Snakebite envenomation is a major public health concern, particularly in low‐ and middle‐income regions where access to safe and effective antivenoms is limited. Traditional antivenoms, derived from immunization with crude venom, often trigger adverse reactions and lack specificity against key venom components.
Hanan Maoz, Amir Elalouf
wiley   +1 more source

Postdiphtheritic acute flaccid paralysis: An epidemiological investigation report

, 2013
A 10-year-old girl presented with faucial diphtheria, 2 weeks following which she presented with acute flaccid paralysis (AFP). The case was notified to the district polio surveillance officer and was epidemiologically investigated.
Namratha Kulkarni, Umesh S Charantimath, Vijaya A Naik, Nikhil P Hawal   +3 more
core   +1 more source

Acute flaccid paralysis in a patient with sacral dimple

World Journal of Clinical Pediatrics, 2013
Sacral dimples are the most common cutaneous anomaly detected during neonatal spinal examination. Congenital dermal sinus tract, a rare type of spinal dysraphism, occurs along the midline neuraxis from occiput down to the sacral region. It is often diagnosed in the presence of a sacral dimple together with skin signs, local infection, meningitis ...
Mohammed, Mostafa, Nehad, Nasef, Tarik, Barakat, Amany K, El-Hawary, Hesham, Abdel-Hady   +4 more
openaire   +2 more sources

Multi‐Omics Landscape of Paraspinal Muscles in Spinal Muscular Atrophy With Scoliosis

Journal of Cellular and Molecular Medicine, Volume 30, Issue 13, July 2026.
ABSTRACT Most spinal muscular atrophy (SMA) patients develop severe scoliosis by late adolescence. Given that the paraspinal muscles—particularly the multifidus—are indispensable for maintaining spinal stability, their site‐specific multi‐omics characteristics in SMA remain insufficiently defined. Herein, integrated multi‐omics sequencing was performed
Zhen Wang, Junduo Zhao, Xu'an Huang, Weiyun Chen, Jianxiong Shen   +4 more
wiley   +1 more source

Reversible electrophysiological abnormalities in acute secondary hyperkalemic paralysis

Annals of Indian Academy of Neurology, 2012
Hyperkalemia manifests clinically with acute neuromuscular paralysis, which can simulate Guillain Barré syndrome (GBS) and other causes of acute flaccid paralysis.
Karkal R Naik, Aralikatte O Saroja, Mallikarjun S Khanpet   +2 more
doaj   +1 more source

Acute Flaccid Paralysis Associated with Novel Enterovirus C105

, 2015
An outbreak of acute flaccid paralysis among children in the United States during summer 2014 was tentatively associated with enterovirus D68 infection. This syndrome in a child in fall 2014 was associated with enterovirus C105 infection. The presence of
Ronald B. Turner, J. Nicholas Brenton, Liana M. Horner, Melinda D. Poulter   +3 more
core   +1 more source

Clinical and biochemical spectrum of hypokalemic paralysis in North: East India

Annals of Indian Academy of Neurology, 2013
Background: Acute hypokalemic paralysis, characterized by acute flaccid paralysis is primarily a calcium channelopathy, but secondary causes like renal tubular acidosis (RTA), thyrotoxic periodic paralysis (TPP), primary hyperaldosteronism, Gitelman′s ...
Ashok K Kayal, Munindra Goswami, Marami Das, Rahul Jain   +3 more
doaj   +1 more source

Acute flaccid myelitis : interim considerations for clinical management [PDF]

Posted November 7, 2014Please note: these considerations are intended to apply to \u201cacute flaccid myelitis\u201d as defined in the document, and are not intended to be generalized to all forms or etiologies of childhood acute flaccid paralysis, such ...

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