![](images/graphics/blank.gif)
Progressive disorder
-
Vulvar and vaginal melanoma (VuM & VaM) is a rare gynecologic malignancy with high mortality but low effectiveness to checkpoint immunotherapy compared to cutaneous melanoma. This article aims to elucidate the role of the disordered immune microenvironment in cancer progression in VuM.
12p
vikoch
27-06-2024
2
1
Download
-
Updating researchers on phenomenal progress in the field of molecular medicine the Encyclopedia of Medical Genomics and Proteomics offers trail-blazing studies and authoritative contributions from more than 400 specialists. Topics include: Molecular diagnostics; Genomics, microbiology, genetics, and pharmacogenetics; Management of infectious, neoplastic, and genetic diseases;...
1391p
vimeyers
29-05-2024
3
2
Download
-
Ebook "Complement therapeutics" highlights progress and trends in the rapidly evolving field of complement-related drug discovery and spotlights examples of clinical applications. As an integral part of innate immunity and critical mediator in homeostatic and inflammatory processes, the human complement system has been identified as contributor to a large number of disorders including ocular, cardiovascular, metabolic, autoimmune, and inflammatory diseases as well as in ischemia/reperfusion injury, cancer and sepsis.
323p
ladongphongthanh1008
22-04-2024
3
3
Download
-
In ebook "Myosins: A superfamily of molecular motors" the association of myosins with diseases including neurological disorders, immunodeficiencies, cardiomyopathies, hearing and vision loss testify to the importance of understanding the biochemical properties and cellular roles of myosins. The 16 chapters in this volume summarize the tremendous progress made in studying members of the myosin superfamily in recent years and offer critical insight into what future research will yield.
498p
ladongphongthanh1008
22-04-2024
5
2
Download
-
In patients with end-stage chronic kidney failure, there are a number of disorders that cause bone damage. In particular, secondary hyperparathyroidism (SHPT) is related to chronic kidney failure, a calcium-phosphorus metabolism disorder that causes bone disorder.
6p
vioraclene
31-03-2024
3
1
Download
-
Macular telangiectasia type 2 (MacTel) is a rare, heritable and largely untreatable retinal disorder, often comorbid with diabetes. Genetic risk loci subtend retinal vascular calibre and glycine/serine/threonine metabolism genes.
11p
vibransone
28-03-2024
9
2
Download
-
Ebook "Unimolecular and supramolecular electronics I: Chemistry and physics meet at metal-molecule interfaces" bring together many of the leading practitioners of the art (in each case I mention only the main author). Bassler sets in order the theoretical understanding of electron transport in disordered (semi)-conducting polymers. Saito summarizes in fantastic detail the progress in understanding charge-transfer crystals and organic superconductivity.
317p
coduathanh1122
27-03-2024
1
1
Download
-
Ebook "Unimolecular and supramolecular electronics II: Chemistry and physics meet at metal-molecule interfaces" bring together many of the leading practitioners of the art (in each case mention only the main author). Bassler sets in order the theoretical understanding of electron transport in disordered (semi)-conducting polymers. Saito summarizes in fantastic detail the progress in understanding charge-transfer crystals and organic superconductivity.
283p
coduathanh1122
27-03-2024
2
1
Download
-
Spinal muscular atrophy is a genetic disorder characterized by degeneration of lower motor neurons, leading to progressive muscular atrophy and even paralysis. Spinal muscular atrophy usually associated with a defect of the survival motor neuron 1 (SMN-1) gene.
5p
vigojek
02-02-2024
5
1
Download
-
The relatively isolated atrophy of the temporal lobes leads to a clinical radiological pattern, referred to as the temporal variant of frontotemporal dementia. While semantic dementia and behavioral variant frontotemporal dementia are classically related to this syndrome, the logopenic variant of primary progressive aphasia has been less commonly reported.
8p
vigojek
02-02-2024
2
1
Download
-
Progressive pseudorheumatoid dysplasia is a rare, autosomal recessively inherited, noninflammatory musculoskeletal disorder caused by mutations occurring in the WNT1-inducible signaling pathway protein 3 gene.
5p
vilazada
31-01-2024
2
2
Download
-
Adult-onset leukoencephalopathies are a group of heterogeneous disorders characterized by white matter abnormalities. Leukoencephalopathy is usually encountered in children, but here we report a case with adultonset leukoencephalopathy. Also, we explore this concept of uncertainty in medicine by discussing the approach to this case that has multiple possible etiologies.
5p
vilazada
31-01-2024
3
2
Download
-
Facial onset sensory and motor neuropathy is a very rare sensorimotor disorder characterized by facial onset and gradual progression, with approximately 100 cases reported worldwide in 2020. We report on our experience with a facial onset sensory and motor neuropathy case in our outpatient pain clinic.
3p
vilazada
31-01-2024
4
2
Download
-
Hyaline fibromatosis syndrome is a rare progressive autosomal recessive connective tissue disorder caused by a mutation in the ANTXR2/CMG2 gene. According to its severity, patients may present with skin nodules or visceral infiltration, which carries a poor prognosis.
6p
vitiki
30-01-2024
5
2
Download
-
Copenhagen syndrome (CS) is a rare disorder mostly observed in adolescent. The onset of the disease, with a progressive anterior vertebral ankylosis in the thoracic and/or lumbar areas often clinically revealed by thoracolumbar kyphosis. We report a series of three patients of CS with good outcome.
6p
vitiki
30-01-2024
4
2
Download
-
Histiocytic sarcoma (HS) is defined as neoplasm resembling morphological and immunophenotypic characteristics of mature histiocytes. It is a rare form of lymphoid neoplasms. Despite advances in treatment and diagnosis of histiocytic sarcoma, majority of cases had poor prognosis due to progressive nature of the disease.
9p
vitiki
30-01-2024
4
2
Download
-
A case of Rasmussen encephalitis in a 8 year old child is reported here who presented with recurrent focal seizures and progressive weakness of left half of body. EEG showed electrical features of epilepsy. MRI brain showed cortical atrophy of one brain hemisphere. On the basis of clinical and radiological evidence, diagnosis of Rasmussen encephalitis was made which is a rare neurological disorder of childhood.
3p
vikissinger
21-12-2023
6
1
Download
-
Anaplastic thyroid carcinoma (ATC) was a rare malignancy featured with the weak immunotherapeutic response. So far, disorders of immunogenic cell death genes (ICDGs) were identified as the driving factors in cancer progression, while their roles in ATC remained poorly clear.
14p
vileonardodavinci
23-12-2023
4
2
Download
-
Myelodysplastic Neoplasms (MDS) are clonal stem cell disorders characterized by ineffective hematopoiesis and progression to acute myeloid leukemia, myelodysplasia-related (AML-MR). A major mechanism of pathogenesis of MDS is the aberration of the epigenetic landscape of the hematopoietic stem cells and/or progenitor cells, especially DNA cytosine methylation, and demethylation.
18p
vialfrednobel
23-12-2023
4
3
Download
-
To access the anxiety rate based on the GAD-7 scale in hypertensive patients being treated at Can Tho Traditional Medicine Hospital and to survey the related factor of anxiety in patients with hypertension at this hospital. Materials and method: Crosssectional study on 110 hypertensive patients at Can Tho Traditional Medicine Hospital from April 2022 to April 2023.
7p
vispacex
16-11-2023
3
1
Download
CHỦ ĐỀ BẠN MUỐN TÌM
![](images/graphics/blank.gif)