Sadia Tabassum
Overview
Explore the profile of Sadia Tabassum including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
32
Citations
238
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Qazi S, Meerza S, Lakhani S, Dogar S, Padhani Z, Mirani M, et al.
PLOS Glob Public Health
. 2024 Sep;
4(9):e0003327.
PMID: 39264889
Approximately five billion people do not have access to necessary surgical treatment globally and up to 85% of children in LMICs are affected with conditions requiring surgical care by the...
2.
Rooman M, Assad Y, Tabassum S, Sultan S, Ayaz S, Khan M, et al.
PLoS One
. 2024 Jul;
19(7):e0307183.
PMID: 38985798
[This corrects the article DOI: 10.1371/journal.pone.0255138.].
3.
Saleh M, Hamhom A, Al-Otaibi A, Alghamdi M, Housawi Y, Aljadhai Y, et al.
Pediatr Neurol
. 2024 Apr;
155:149-155.
PMID: 38653183
Background: Neuronal ceroid lipofuscinoses (NCLs) represent a heterogeneous group of inherited metabolic lysosomal disorders characterized by neurodegeneration. This study sought to describe the clinical and molecular characteristics of NCLs in...
4.
Almuqbil M, Tabassum S, Muthaffar O, Ghamdi F, Al Masseri Z, Alsaman A, et al.
Ann Clin Transl Neurol
. 2024 Feb;
11(4):1063-1066.
PMID: 38389300
Parkinsonism-dystonia-2 PKDYS2 is an autosomal-recessive disorder, caused by pathogenic biallelic variants in SLC18A2 which encodes the vesicular monoamine transporter (VMAT2) protein. PKDYS2 is a treatable neurotransmitter disease, and the rate...
5.
Bibi S, Abbas G, Khan M, Nawaz T, Ullah Q, Uddin A, et al.
Front Endocrinol (Lausanne)
. 2023 Sep;
14:1093353.
PMID: 37674615
Introduction: Polycystic Ovarian Syndrome (PCOS) is a globally prevalent condition that leads to infertility in women. While environmental factors contribute to PCOS, maternal genetics also play a significant role. Currently,...
6.
Alharbi R, Kaki A, Tabassum S
Cureus
. 2023 Jul;
15(6):e40735.
PMID: 37485175
Background Status epilepticus (SE) is one of the most common and well-known neurological emergencies in pediatrics, especially among kids under two years of age. Early identification and treatment are crucial...
7.
Qazi S, Meerza S, Groen R, Dogar S, Mirani M, Jamali M, et al.
PLOS Glob Public Health
. 2023 Mar;
2(12):e0000810.
PMID: 36962776
Surgical conditions are responsible for up to 15% of total Disability-Adjusted Life Years (DALY) lost globally. Approximately 4.8 billion people have no access to surgical care and this studies aim...
8.
Almutairi M, Tabassum S
Cureus
. 2022 Dec;
14(11):e31019.
PMID: 36475157
Congenital insensitivity to pain with anhidrosis, or hereditary sensory and autonomic neuropathy (HSAN) type IV, is an exceedingly rare neurogenetic disorder. Reported causes are homozygous or compound heterozygous loss-of-function mutations...
9.
Aldhilan A, Alhakeem A, Al Hajjaj S, Abukhalid M, Aldhalaan H, Salah E, et al.
Pediatr Neurol
. 2022 Jul;
134:78-82.
PMID: 35841715
Background: Hyperekplexia is a rare disorder characterized by exaggerated startle responses to unexpected sensory stimuli, recurrent apneas, and stiffness. Only few studies have been published on this disorder in populations...
10.
Javed S, McClure J, Ali Syed M, Obasuyi O, Ali S, Tabassum S, et al.
PLoS One
. 2022 May;
17(5):e0268152.
PMID: 35512008
Buffalo represent a major source of milk in Pakistan. However, production is impacted by the disease bovine mastitis. Mastitis causes significant economic losses, with Staphylococcus aureus (S. aureus) being one...