Muhammad Zeeshan Ali
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Explore the profile of Muhammad Zeeshan Ali including associated specialties, affiliations and a list of published articles.
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26
Citations
71
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Recent Articles
1.
Ahmad S, Muurinen M, Loid P, Ali M, Muzammal M, Fatima S, et al.
Bone Rep
. 2024 Nov;
22:101789.
PMID: 39540058
Multicentric osteolysis nodulosis and arthropathy (MONA) is a rare skeletal dysplasia characterized primarily by progressive osteolysis, particularly affecting the carpal and tarsal bones, accompanied by osteoporosis. In addition, it features...
2.
Hashmi J, Latif M, Balahmar R, Ali M, Alfadhli F, Khan M, et al.
Front Genet
. 2024 Sep;
15:1421943.
PMID: 39280098
Background: α-mannosidosis (MAN) is a rare genetic condition that segregates in an autosomal recessive manner. Lack of lysosomal alpha-mannosidase is the underlying cause of the disease. Symptoms of the disease...
3.
Ullah F, Ali M, Ahmad S, Muzammal M, Khan S, Khan J, et al.
Nucleosides Nucleotides Nucleic Acids
. 2024 May;
:1-24.
PMID: 38718411
Usher syndrome (USH) is a genetic disorder that is characterized by sensorineural hearing loss (HL) and visual abnormality, i.e., loss of night vision and side (peripheral) vision. Usher syndrome is...
4.
Ahmad S, Ali M, Muzammal M, Khan A, Ikram M, Muurinen M, et al.
Genes (Basel)
. 2023 Apr;
14(4).
PMID: 37107627
Polydactyly is a rare autosomal dominant or recessive appendicular patterning defect of the hands and feet, phenotypically characterized by the duplication of digits. Postaxial polydactyly (PAP) is the most common...
5.
Ali M, Asghar A, Slehria A, Aquil H
J Pak Med Assoc
. 2023 Apr;
73(4):922-924.
PMID: 37052017
Lymphangiomas, also known as lymphatic malformations, are rare non-neoplastic lesions of vascular origin showing lymphatic differentiation. These are most commonly reported in children within the neck and axillary region; however,...
6.
Nawaz M, Nawaz H, Majeed M, Rashid N, Javed M, Naz S, et al.
Photodiagnosis Photodyn Ther
. 2023 Mar;
42:103532.
PMID: 36963645
Background: Surface-enhanced Raman spectroscopy (SERS) is an efficient technique which has been used for the analysis of filtrate portions of serum samples of Hepatitis B (HBV) and Hepatitis C (HCV)...
7.
Ahmad S, Ali M, Abbasi S, Abbas S, Ahmed I, Abbas S, et al.
Front Endocrinol (Lausanne)
. 2023 Mar;
14:1066182.
PMID: 36960394
Background: Isolated growth hormone deficiency (IGHD) is caused by a severe shortage or absence of growth hormone (GH), which results in aberrant growth and development. Patients with IGHD type IV...
8.
Akram M, Majeed M, Nawaz H, Rashid N, Javed M, Ali M, et al.
Photodiagnosis Photodyn Ther
. 2022 Nov;
40:103199.
PMID: 36371020
Background: Surface-enhanced Raman spectroscopy (SERS) is explored to design a rapid screening method for the characterization and diagnosis of typhoid fever by employing filtrate fractions of blood serum samples obtained...
9.
Raza A, Parveen S, Majeed M, Nawaz H, Javed M, Iqbal M, et al.
Spectrochim Acta A Mol Biomol Spectrosc
. 2022 Oct;
285:121903.
PMID: 36209714
Surface-enhanced Raman spectroscopy (SERS) is used to identify the biochemical changes associated with the antifungal activities of selenium and zinc organometallic complexes against Aspergillus niger fungus. These biochemical changes identified...
10.
Ahmad S, Ali M, Muzammal M, Mir F, Khan M
Mol Genet Genomics
. 2022 Jul;
297(5):1195-1214.
PMID: 35907958
Disorders that result from de-arrangement of growth, development and/or differentiation of the appendages (limbs and digit) are collectively called as inherited abnormalities of human appendicular skeleton. The bones of appendicular...