Alíz Zimmermann

发表

Seizure-Induced Alterations in Cerebrovascular Function in the Neonate

Ferenc Domoki, Ferenc Bari, F. Bari, 2008, Developmental Neuroscience.

Epileptic seizures increase circulating endothelial cells in peripheral blood as early indicators of cerebral vascular damage.

C. Leffler, Alíz Zimmermann, H. Parfenova, 2010, American journal of physiology. Heart and circulatory physiology.

PACAP and VIP differentially preserve neurovascular reactivity after global cerebral ischemia in newborn pigs

G. Toth, D. Busija, F. Bari, 2009, Brain Research.

Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

T. Mazza, S. Castellana, E. Valente, 2014, Orphanet Journal of Rare Diseases.

Secretory phospholipase A2 inhibitor PX-18 preserves microvascular reactivity after cerebral ischemia in piglets.

J. Pardeike, R. Müller, F. Bari, 2009, Microvascular research.

Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III

J. Yates, A. Vanderver, D. Timmann, 2015, Nature Communications.

Acetazolamide induces indomethacin and ischaemia‐sensitive pial arteriolar vasodilation in the piglet

D. Busija, F. Bari, F. Domoki, 2008, Acta paediatrica.

Further delineation of the phenotype of PAK3-associated x-linked intellectual disability: Identification of a novel missense mutation and review of literature.

L. Armengol, M. Széll, Alíz Zimmermann, 2020, European journal of medical genetics.

Hydrogen is Neuroprotective and Preserves Cerebrovascular Reactivity in Asphyxiated Newborn Pigs

F. Bari, F. Domoki, I. Nemeth, 2010, Pediatric Research.

Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability

T. Kalmár, L. Sztriha, A. Máté, 2018, Journal of Human Genetics.

Reventilation with room air or 100% oxygen after asphyxia differentially affects cerebral neuropathology in newborn pigs

F. Bari, F. Domoki, G. Cserni, 2006, Acta paediatrica.

A Novel Homozygous Frameshift WDR81 Mutation associated with Microlissencephaly, Corpus Callosum Agenesis, and Pontocerebellar Hypoplasia

T. Kalmár, L. Sztriha, A. Máté, 2020, Journal of Pediatric Genetics.

Tremor as an early sign of hereditary spastic paraplegia due to mutations in ALDH18A1

T. Kalmár, L. Sztriha, Alíz Zimmermann, 2020, Brain and Development.

Spectrum of Neurodevelopmental Disabilities

L. Sztriha, A. Máté, Alíz Zimmermann, 2015, Journal of child neurology.

A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder

N. Nagy, Alíz Zimmermann, András Salamon, 2024, BMC pediatrics.

Cerebroprotective effects of the CO-releasing molecule CORM-A1 against seizure-induced neonatal vascular injury.

C. Leffler, Alíz Zimmermann, H. Parfenova, 2007, American journal of physiology. Heart and circulatory physiology.