Search Results - "Forman EB"

DISC1 mutant macaques capture behavioral and neural hallmarks of psychiatric disease.

Authors: Zhou, Wenjia Sun, Jiayu Zuo, Guo-Long et al.

Source: National Science Review. Apr2026, Vol. 13 Issue 8, p1-14. 14p.

Patient-specific automated cerebrospinal fluid pressure control to augment spinal wound closure: a case series using the LiquoGuard®.

Authors: Khan, Danyal Z. Tariq, Kanza Lee, Keng Siang et al.

Source: British Journal of Neurosurgery. Aug2025, Vol. 39 Issue 4, p476-484. 9p.

A pseudo‐homozygous missense variant and Alu‐mediated exon 5 deletion in FARS2 causing spastic paraplegia 77.

Authors: Lin, Shu‐Huai Xie, Jun‐Hao Jiang, Jun‐Yi et al.

Source: Annals of Clinical & Translational Neurology. Nov2024, Vol. 11 Issue 11, p3019-3024. 6p.

Clinical utility of periodic reinterpretation of CNVs of uncertain significance: an 8-year retrospective study.

Authors: Ravel, Jean-Marie Renaud, Mathilde Muller, Jean et al.

Source: Genome Medicine. 5/23/2023, Vol. 15 Issue 1, p1-10. 10p.

Immunity in neuromodulation: probing neural and immune pathways in brain disorders.

Authors: Hours, C. Vayssière, Pia Gressens, P. et al.

Source: Journal of Neuroinflammation. 4/28/2025, Vol. 22 Issue 1, p1-38. 38p.

Idiopathic intracranial hypertension presenting as iron deficiency anemia: a case report.

Authors: Sim, Peng Yong Taribagil, Priyal Woollacott, Ione O. C. et al.

Source: Journal of Medical Case Reports. 2/2/2021, Vol. 15 Issue 1, p1-6. 6p.

The Association Between Anemia and Pseudotumor Cerebri.

Authors: Gibbons AB Li X Henderson AD

Corporate Authors: Gibbons AB Li X Henderson AD

Source: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society [J Neuroophthalmol] 2026 Apr 22. Date of Electronic Publication: 2026 Apr 22.

Publication Type: Journal Article

Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 9431308 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1536-5166 (Electronic) Linking ISSN: 10708022 NLM ISO Abbreviation: J Neuroophthalmol Subsets: MEDLINE

Genetic analysis reveals phenotypic variability in three Colombian families with dopa-responsive dystonia: novel genotype-phenotype correlations.

Authors: Lince-Rivera I Martinez-Córdoba N Ramón-Gómez JL et al.

Source: BMC medical genomics [BMC Med Genomics] 2026 Apr 11; Vol. 19 (1). Date of Electronic Publication: 2026 Apr 11.

Publication Type: Journal Article; Case Reports

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794 (Electronic) Linking ISSN: 17558794 NLM ISO Abbreviation: BMC Med Genomics Subsets: MEDLINE

Exploring the clinical significance of anemia in idiopathic intracranial hypertension.

Authors: Tutar, Nurhan Kaya Yerturk, Mehmet Omerhoca, Sami et al.

Source: Turkish Journal of Neurology / Türk Nöroloji Dergisi. Dec2024, Vol. 30 Issue 4, p220-224. 5p.

Diagnostic Limitations in Congenital Zika Virus Infection.

Authors: Flanagan M Hughes H Forman EB et al.

Source: Irish medical journal [Ir Med J] 2020 Jun 11; Vol. 113 (6), pp. 101. Date of Electronic Publication: 2020 Jun 11.

Publication Type: Case Reports; Journal Article

Journal Info: Publisher: Irish Medical Association Country of Publication: Ireland NLM ID: 0430275 Publication Model: Electronic Cited Medium: Internet ISSN: 0332-3102 (Print) Linking ISSN: 03323102 NLM ISO Abbreviation: Ir Med J Subsets: MEDLINE

Increased Ca²⁺ signaling in NRXN1α^+/- neurons derived from ASD induced pluripotent stem cells.

Authors: Avazzadeh S McDonagh K Reilly J et al.

Source: Molecular autism [Mol Autism] 2019 Dec 30; Vol. 10, pp. 52. Date of Electronic Publication: 2019 Dec 30 (Print Publication: 2019).

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101534222 Publication Model: eCollection Cited Medium: Internet ISSN: 2040-2392 (Electronic) NLM ISO Abbreviation: Mol Autism Subsets: MEDLINE

Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases.

Authors: Alfieri, Paolo Scibelli, Francesco Sinibaldi, Lorenzo et al.

Source: Genes, Brain & Behavior. Sep2020, Vol. 19 Issue 7, p1-9. 9p.

Benefit of high‐dose oral riboflavin therapy in riboflavin transporter deficiency.

Authors: Fennessy, Jack R. Cornett, Kayla M. D. Burns, Joshua et al.

Source: Journal of the Peripheral Nervous System. Sep2023, Vol. 28 Issue 3, p308-316. 9p.

A review of antipsychotic therapy effectiveness and tolerability among individuals with copy number variants relevant to schizophrenia.

Authors: Colijn MA; Department of Psychiatry.; Mathison Centre for Mental Health Research and Education.; Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada.

Source: Psychiatric genetics [Psychiatr Genet] 2025 Jun 01; Vol. 35 (3), pp. 37-43. Date of Electronic Publication: 2025 Mar 25.

Publication Type: Journal Article; Review

Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9106748 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1473-5873 (Electronic) Linking ISSN: 09558829 NLM ISO Abbreviation: Psychiatr Genet Subsets: MEDLINE

Neuropathy-associated Fars2 deficiency affects neuronal development and potentiates neuronal apoptosis by impairing mitochondrial function.

Authors: Chen, Xihui Liu, Fangfang Li, Bowen et al.

Source: Cell & Bioscience. 7/6/2022, Vol. 12 Issue 1, p1-23. 23p.

Diagnosis of idiopathic intracranial hypertension - the importance of excluding secondary causes: A systematic review.

Authors: Kilic, Kubra Korsbæk, Johanne Juhl Jensen, Rigmor H et al.

Source: Cephalalgia. May2022, Vol. 42 Issue 6, p524-541. 18p.

UBA1 and DNMT3A mutations in VEXAS syndrome. A case report and literature review.

Authors: Shaukat, Farah Hart, Melissa Burns, Timothy et al.

Source: Modern Rheumatology Case Reports. Jan2022, Vol. 6 Issue 1, p134-139. 6p.

NRXN1α^+/- is associated with increased excitability in ASD iPSC-derived neurons.

Authors: Avazzadeh, Sahar Quinlan, Leo R. Reilly, Jamie et al.

Source: BMC Neuroscience. 9/15/2021, Vol. 22 Issue 1, p1-14. 14p.

Breaking a single hydrogen bond in the mitochondrial tRNA^Phe‐PheRS complex leads to phenotypic pleiotropy of human disease.

Authors: Peretz, Moshe Tworowski, Dmitry Kartvelishvili, Ekaterine et al.

Source: FEBS Journal. Sep2020, Vol. 287 Issue 17, p3814-3826. 13p.

Riboflavin - properties, occurrence and its use in medicine.

Authors: Szczuko, Małgorzata Ziętek, Maciej Kulpa, Danuta et al.

Source: Pteridines. Feb2019, Vol. 30 Issue 1, p33-47. 15p.