A rare case of centronuclear myopathy with DNM2 mutation: genotype–phenotype correlation

por Aghbolaghi, Amir Ghorbani, Lechpammer, Mirna
Publicado 2017

Molecular Genetics of Intracranial Meningiomas with Emphasis on Canonical Wnt Signalling

por Pećina-Šlaus, Nives, Kafka, Anja, Lechpammer, Mirna
Publicado 2016

Inhibition of HIF2α Is Sufficient to Suppress pVHL-Defective Tumor Growth

por Kondo, Keiichi, Kim, William Y, Lechpammer, Mirna, Kaelin, William G
Publicado 2003

Hidden treasures: Incidental findings in two cases of chronic subdural hematoma

por Ladenheim, Alexander, Mitra, Ananya Datta, Lechpammer, Mirna, Dwyre, Denis M.
Publicado 2022

Giant cell reparative granuloma of the sphenoid: Case report and review of the literature

por Jamil, Osama A., Lechpammer, Mirna, Prasad, Sashank, Litvack, Zachary, Dunn, Ian F.
Publicado 2012

Ectopic Acromegaly Arising from a Pituitary Adenoma within the Bony Intersphenoid Septum of a Patient with Empty Sella Syndrome

por Arzamendi, Audrey E., Shahlaie, Kiarash, Latchaw, Richard E., Lechpammer, Mirna, Arzumanyan, Hasmik
Publicado 2016

Abnormal white matter tracts resembling pencil fibers involving prefrontal cortex (Brodmann area 47) in autism: a case report

por Hashemi, Ezzat, Ariza, Jeanelle, Lechpammer, Mirna, Noctor, Stephen C., Martínez-Cerdeño, Verónica
Publicado 2016

Chondroblastoma of the Clivus: Case Report and Review

por Liu, Jonathan, Ahmadpour, Arjang, Bewley, Arnaud F., Lechpammer, Mirna, Bobinski, Matthew, Shahlaie, Kiarash
Publicado 2015

FMR1 premutation with Prader–Willi phenotype and fragile X‐associated tremor/ataxia syndrome

por Martínez‐Cerdeño, Verónica, Lechpammer, Mirna, Noctor, Stephen, Ariza, Jeanelle, Hagerman, Paul, Hagerman, Randi
Publicado 2017

Expression Levels and Localizations of DVL3 and sFRP3 in Glioblastoma

por Kafka, Anja, Tomas, Davor, Lechpammer, Mirna, Gabud, Tea, Pažanin, Leo, Pećina-Šlaus, Nives
Publicado 2017

PATH-31. THE IMPACT OF MOLECULAR PROFILING OF PEDIATRIC CNS TUMORS ON TUMOR DIAGNOSIS AND MANAGEMENT - A SINGLE CENTER EXPERIENCE

por Sabet, Kazuhiro, Zwienenberg, Marike, Lechpammer, Mirna, Jin, Lee-Way, Solomon, David, Kline, Cassie, Antony, Reuben
Publicado 2020

An extremely rare case of concurrent BRAF V600E mutation driven hairy cell leukemia and melanoma: case report and review of literature

por Ghorbani-Aghbolaghi, Amir, Lechpammer, Mirna, Ali, Saba F., Ku, Nam K., Dwyre, Denis M., Rashidi, Hooman H.
Publicado 2017

Reciprocal H3.3 gene editing identifies K27M and G34R mechanisms in pediatric glioma including NOTCH signaling

por Chen, Kuang-Yui, Bush, Kelly, Klein, Rachel Herndon, Cervantes, Vanessa, Lewis, Nichole, Naqvi, Aasim, Carcaboso, Angel M., Lechpammer, Mirna, Knoepfler, Paul S.
Publicado 2020

Congenital presentation of synchronous Atypical Teratoid Rhabdoid Tumor and Malignant Rhabdoid Tumor of the urinary bladder in a term infant

por Tang, Vivian, Conner, Peter Michael, Tovar, Jason Paul, Gandour-Edwards, Regina Frances, Antony, Reuben, Bobinski, Matthew, Edwards, Michael Steven Brent, Lechpammer, Mirna
Publicado 2020

Advances in Immunotherapy for the Treatment of Adult Glioblastoma: Overcoming Chemical and Physical Barriers

por Lechpammer, Mirna, Rao, Rohan, Shah, Sanjit, Mirheydari, Mona, Bhattacharya, Debanjan, Koehler, Abigail, Toukam, Donatien Kamdem, Haworth, Kevin J., Pomeranz Krummel, Daniel, Sengupta, Soma
Publicado 2022

Microscopy with ultraviolet surface excitation for rapid slide-free histology

por Fereidouni, Farzad, Harmany, Zachary T., Tian, Miao, Todd, Austin, Kintner, John A., McPherson, John D., Borowsky, Alexander D., Lechpammer, Mirna, Bishop, John, Demos, Stavros G., Levenson, Richard
Publicado 2017

Exposure to DMSO during infancy alters neurochemistry, social interactions, and brain morphology in long‐evans rats

por Rabow, Zachary, Morningstar, Taryn, Showalter, Megan, Heil, Hailey, Thongphanh, Krista, Fan, Sili, Chan, Joanne, Martínez‐Cerdeño, Verónica, Berman, Robert, Zagzag, David, Nudler, Evgeny, Fiehn, Oliver, Lechpammer, Mirna
Publicado 2021

Concomitant occurrence of FXTAS and clinically defined sporadic inclusion body myositis: report of two cases

por Lechpammer, Mirna, Martínez Cerdeńo, Verónica, Hunsaker, Michael Ryan, Hah, Mina, Gonzales, Hilary, Tisch, Steve, Joffe, Ronald, Pamphlett, Roger, Tassone, Flora, Hagerman, Paul J., Bolitho, Samuel J., Hagerman, Randi J.
Publicado 2017

Extracellular GAPDH Promotes Alzheimer Disease Progression by Enhancing Amyloid-β Aggregation and Cytotoxicity

por Lazarev, Vladimir F, Tsolaki, Magda, Mikhaylova, Elena R, Benken, Konstantin A, Shevtsov, Maxim A, Nikotina, Alina D, Lechpammer, Mirna, Mitkevich, Vladimir A, Makarov, Alexander A, Moskalev, Alexey A, Kozin, Sergey A, Margulis, Boris A, Guzhova, Irina V, Nudler, Evgeny
Publicado 2021

Genomic Profiling Reveals Differences in Primary Central Nervous System Lymphoma and Large B-Cell Lymphoma, With Subtyping Suggesting Sensitivity to BTK Inhibition

por Severson, Eric A, Haberberger, James, Hemmerich, Amanda, Huang, Richard S P, Edgerly, Claire, Schiavone, Kelsie, Najafian, Adib, Hiemenz, Matthew, Lechpammer, Mirna, Vergilio, Jo-Anne, Lesser, Glenn, Strowd, Roy, Elvin, Julia, Ross, Jeffrey S, Hegde, Priti, Alexander, Brian, Singer, Samuel, Ramkissoon, Shakti
Publicado 2023