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Osteoprotegerin genetic polymorphisms and their influence on therapeutic response to ibandronate in postmenopausal osteoporotic females.
Not available
S-EPMC10521989
|
biostudies-literature
Cite
Novel missense mutation in the RSPO4 gene in congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I).
Not available
S-EPMC3532313
|
biostudies-literature
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Exome sequencing reveals broad genetic heterogeneity for neuromuscular disorders in consanguineous Pakistani Families.
Not available
S-EPMC12480867
|
biostudies-literature
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Comparison of a single session of tDCS on cerebellum vs. motor cortex in stroke patients: a randomized sham-controlled trial.
Not available
S-EPMC10732189
|
biostudies-literature
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Short term effects of anodal cerebellar vs. anodal cerebral transcranial direct current stimulation in stroke patients, a randomized control trial.
Not available
S-EPMC9730515
|
biostudies-literature
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Computational analysis of functional single nucleotide polymorphisms associated with SLC26A4 gene.
Not available
S-EPMC6977751
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biostudies-literature
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Concomitant use of blinatumomab and donor lymphocyte infusion for mixed-phenotype acute leukemia: a case report with literature review.
Not available
S-EPMC6439498
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biostudies-literature
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Genetic Investigation and Transcriptome Profiling in a Nuclear Family With Peutz–Jeghers Syndrome
Not available
S-EPMC12373473
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biostudies-literature
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Colibactin possessing E. coli isolates in association with colorectal cancer and their genetic diversity among Pakistani population.
Not available
S-EPMC9651576
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biostudies-literature
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A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency.
Not available
S-EPMC4292821
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biostudies-literature
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