Mohammad Keramatipour
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Explore the profile of Mohammad Keramatipour including associated specialties, affiliations and a list of published articles.
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67
Citations
333
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Recent Articles
1.
Rafiee M, Razipour M, Keramatipour M, Roozbeh J, Entezam M
J Appl Genet
. 2025 Feb;
PMID: 39951171
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited renal disorder, primarily caused by mutations in the PKD1 and PKD2. Genetic testing is valuable for the diagnosis, prognosis,...
2.
Amirfiroozy A, Naghinejad M, Rezamand A, Farhangi H, Golchehre Z, Jalali H, et al.
Mol Cell Probes
. 2025 Jan;
79:102014.
PMID: 39875016
Osteopetrosis is a group of genetically and clinically diverse inherited disorders characterized by an increase in bone density. The main known cause is an abnormality in the development or function...
3.
Jamee M, Sharafian S, Eslami N, Bayegi S, Keramatipour M, Nabavi M, et al.
Allergol Immunopathol (Madr)
. 2024 Sep;
52(5):6-14.
PMID: 39278845
Background: Elevated level of double-negative T (DNT) cells is a historical hallmark of autoimmune lymphoproliferative syndrome (ALPS) diagnosis. However, the peripheral blood level of DNT cells might also be compromised...
4.
Karimzade P, Eghbali A, Keramatipour M, Shiari R, Golchehre Z, Taghizadeh M, et al.
Case Reports Immunol
. 2024 Aug;
2024:4380689.
PMID: 39161369
Background: Adenosine deaminase deficiency 2 (DADA2) is an autoinflammatory disorder, caused by the gene mutation. The major clinical manifestations include recurrent vasculitis, neurological disorders such as stroke, hematologic abnormalities, and...
5.
Tasharrofi B, Karimzadeh P, Asadollahi M, Hasani S, Heidari M, Keramatipour M
Iran J Child Neurol
. 2024 Jul;
18(3):117-129.
PMID: 38988838
Objectives: Mutations in the TREX1 gene cause Aicardi-Goutières syndrome (AGS) 1, associated with a spectrum of autoimmune and neurodegenerative manifestations. AGS 1, the most severe neonatal type of AGS, is...
6.
Tasharrofi B, Najafi A, Pourbakhtyaran E, Amirsalari S, Khan G, Ashrafi M, et al.
Mol Biol Rep
. 2024 Jun;
51(1):714.
PMID: 38824264
Background: NOTCH3 variants are known to be linked to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). However, some null NOTCH3 variants with homozygous inheritance cause neurological symptoms...
7.
Nourmohammadi P, Asadollahi M, Karamzade A, Eshaghkhani Y, Babaei M, Golchehre Z, et al.
J Genet
. 2023 Sep;
102.
PMID: 37674283
Vanishing of white matter (VWM) is a hereditary heterogeneous brain disorder that most often affects children. However, the onset of the disease varies from childhood to adulthood. VWM is caused...
8.
Mousavi Khorshidi M, Seeleuthner Y, Chavoshzadeh Z, Behfar M, Hamidieh A, Alimadadi H, et al.
J Clin Immunol
. 2023 Aug;
43(8):1941-1952.
PMID: 37584719
Purpose: Major histocompatibility complex class II (MHC-II) deficiency is a rare inborn error of immunity (IEI). Impaired antigen presentation to CD4 + T cells results in combined immunodeficiency (CID). Patients...
9.
Amirkashani D, Asadollahi M, Hosseini R, Talebi S, Golchehre Z, Keramatipour M
Iran J Child Neurol
. 2023 Apr;
17(2):127-133.
PMID: 37091464
Succinyl-CoA:3-oxoacid CoA-transferase (SCOT) deficiency is an inborn error of ketone body utilization characterized by intermittent ketoacidosis crises. This study reports the first Iranian patient with SCOT deficiency who presented with...
10.
Bazgir N, Tahvildari A, Chavoshzade Z, Jamee M, Golchehre Z, Karimi A, et al.
Allergy Asthma Clin Immunol
. 2023 Apr;
19(1):29.
PMID: 37038193
Background: Caspase-8 is a molecule in the FAS pathway that initiates apoptosis. One of the rarest autoimmune lymphoproliferative syndromes is caspase-8 deficiency. Immunodeficiency, splenomegaly, and lymphadenopathy are the common symptoms...