Search Results - "Greenbaum L"

Editorial: Combination Therapies for MASH: A Step Forward or More Complexity? Authors' Reply.

Authors: Lawitz E Greenbaum L

Source: Alimentary pharmacology & therapeutics [Aliment Pharmacol Ther] 2026 Mar; Vol. 63 (6), pp. 905-906. Date of Electronic Publication: 2025 Dec 26.

Publication Type: Editorial

Journal Info: Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 8707234 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2036 (Electronic) Linking ISSN: 02692813 NLM ISO Abbreviation: Aliment Pharmacol Ther Subsets: MEDLINE; In Process

Author Index.

Source: Nephrology. Oct2022 Supplement S1, Vol. 27, p115-122. 8p.

Rare-Variant Burden across Lysosomal Genes Implicates Sialylation and Ganglioside Metabolism in Parkinson's Disease.

Authors: Senkevich K Parlar SC Chantereault C et al.

Source: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2026 Jun 10. Date of Electronic Publication: 2026 Jun 10.

Publication Type: Journal Article

Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE

The GBA1 p.E427K (p.E388K) Variant Is a Risk Factor for Synucleinopathies: A Meta-Analysis.

Authors: Chifamba LV Parlar SC Somerville EN et al.

Corporate Authors: Chifamba LV Parlar SC Somerville EN et al.

Source: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2026 May 22. Date of Electronic Publication: 2026 May 22.

Publication Type: Journal Article

Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE

The genetic and clinical characteristics of oculopharyngeal muscular dystrophy patients in Israel.

Authors: Ben-David M Greenbaum L Nikitn V et al.

Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2026 May 19; Vol. 21 (1). Date of Electronic Publication: 2026 May 19.

Publication Type: Journal Article

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE; In Process

Dietary management of pediatric patients with kidney disease: recommendations by the Korean Society of Pediatric Nephrology and the Korean Society of Clinical Nutrition.

Authors: Ahn, Yo Han Kang, Hee Gyung Song, Jiyoung et al.

Source: Childhood Kidney Diseases. Feb2026, Vol. 30 Issue 1, p4-14. 11p.

Effect of PI3K-p110α Inhibitor Alpelisib in the Differentiation and Effector Functions of M-CSF and GM-CSF Macrophages.

Authors: Villa-Gómez, Cristina Bermejo, Verónica Márquez-Leiva, Inmaculada et al.

Source: International Journal of Molecular Sciences. May2026, Vol. 27 Issue 10, p4171. 21p.

Multi-cohort, cross-species urinary proteomics reveals signatures of LRRK2 dysfunction in Parkinson's disease.

Authors: Vu, Duc Tung Sibran, William Metousis, Andreas et al.

Source: Molecular Systems Biology. May2026, Vol. 22 Issue 5, p712-737. 26p.

Markers for the Severity of Multisystem Inflammatory Syndrome in Children: A Multivariate Analysis.

Authors: Vasilev, Georgi Gorelyova, Nadzhie Shumnalieva, Russka et al.

Source: International Journal of Pediatrics. 4/10/2026, Vol. 2026, p1-11. 11p.

Ten tips on how to optimize nutrition in children with chronic kidney disease or on dialysis.

Authors: Polderman, Nonnie Shaw, Vanessa Anderson, Caroline E et al.

Source: Clinical Kidney Journal. Apr2026, Vol. 19 Issue 4, p1-13. 13p.

Deficient Visuospatial Incidental and Intentional Memory in Cognitively Healthy Middle-Aged First-Degree Descendants of Alzheimer's Disease Patients.

Authors: Álvarez-Huante, Claudia Guadalupe Rincón-Ortega, María Fernanda Palomares-Vallejo, Edgar Josué et al.

Source: Brain Sciences (2076-3425). Apr2026, Vol. 16 Issue 4, p406. 16p.

Genetic testing for Parkinson's disease in Israel: Insights from the Rostock Parkinson's Disease (ROPAD) study.

Authors: Anis S Weill C Ponger P et al.

Source: Parkinsonism & related disorders [Parkinsonism Relat Disord] 2025 Aug; Vol. 137, pp. 107940. Date of Electronic Publication: 2025 Jun 28.

Publication Type: Journal Article

Journal Info: Publisher: Elsevier Science Country of Publication: England NLM ID: 9513583 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-5126 (Electronic) Linking ISSN: 13538020 NLM ISO Abbreviation: Parkinsonism Relat Disord Subsets: MEDLINE

Clinical profiling and medical management of Israeli individuals with Phelan McDermid syndrome.

Authors: Chorin O Greenbaum L Lev-Hochberg S et al.

Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2025 Mar 18; Vol. 20 (1), pp. 132. Date of Electronic Publication: 2025 Mar 18.

Publication Type: Journal Article

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE

Ocular manifestations and outcomes of OPMD- a report from the national IsrOPMD registry.

Authors: Mekiten O Zvulunov A Ben Simon G et al.

Source: European journal of ophthalmology [Eur J Ophthalmol] 2025 Mar; Vol. 35 (2), pp. 451-455. Date of Electronic Publication: 2024 May 29.

Publication Type: Journal Article; Review

Journal Info: Publisher: SAGE Publishing Country of Publication: United States NLM ID: 9110772 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1724-6016 (Electronic) Linking ISSN: 11206721 NLM ISO Abbreviation: Eur J Ophthalmol Subsets: MEDLINE

Author Index.

Source: Pediatric Transplantation. May2009 Supplement, Vol. 13, p157-167. 11p.

Combined Histological and Proteomic Analysis Reveals Muscle Denervation in KMT5B-Related Neurodevelopmental Disorder: A Case Report.

Authors: Aksel Kilicarslan, Ozge Gangfuß, Andrea Kölbel, Heike et al.

Source: Journal of Clinical Medicine. Dec2025, Vol. 14 Issue 24, p8636. 11p.

Neutropenia Through Enhanced Neutrophil Apoptosis and Secondary Necrosis in Wolfram Syndrome 1.

Alternate Title: Wolfram Sendromu 1'de Artmış Nötrofil Apoptozu ve Sekonder Nekrozuna Bağlı Nötropeni.

Authors: Aslan, Deniz Kayhan, Handan

Source: Turkish Journal of Hematology. 2026, Vol. 43 Issue 1, p96-100. 5p.

YKT6 Is Essential for Male Fertility by Promoting Meiosis Progression During Spermatogenesis of Mice.

Authors: Cen, Jie Yu, Xiaochen Wang, Ziqi et al.

Source: Cell Proliferation. Jan2026, Vol. 59 Issue 1, p1-14. 14p.

Predictors of hyperkalemia in pediatric patients on dialysis: international prospective observational study.

Authors: Paglialonga, Fabio Shroff, Rukshana Zagozdzon, Ilona et al.

Source: Pediatric Nephrology. Aug2025, Vol. 40 Issue 8, p2611-2618. 8p.

Parental germline mosaicism in genome-wide phased de novo variants: Recurrence risk assessment and implications for precision genetic counselling.

Authors: Lecoquierre, François Drouot, Nathalie Coutant, Sophie et al.

Source: PLoS Genetics. 3/31/2025, Vol. 21 Issue 3, p1-18. 18p.