Nicole Wolf
Overview
Explore the profile of Nicole Wolf including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
264
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0
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Recent Articles
1.
Kleiner L, Wolf N, Precht C, Haenssgen K, Forterre F, Duver P
Front Vet Sci
. 2025 Jan;
11:1510253.
PMID: 39881725
Introduction: Sacroiliac luxation is a common traumatic feline injury, with the small size of the sacral body being a challenge for surgical stabilization. This study compared an innovative computer-guided drilling...
2.
Amato M, Darling A, Stovickova L, Attard S, Eggink H, Engelen M, et al.
Eur J Paediatr Neurol
. 2024 Jul;
52:10-19.
PMID: 38970889
Aim: This exploratory study evaluates rating scale usage by experts from the European Reference Network for Rare Neurological Diseases (ERN-RND) for paediatric MD, considering factors like diagnosis, intellectual disability, age,...
3.
Gavazzi F, Patel V, Charsar B, Glanzman A, Erler J, Sevagamoorthy A, et al.
J Child Neurol
. 2023 Jul;
38(8-9):498-504.
PMID: 37461315
pathogenic variants are associated with a spectrum of neurologic impairments including movement disorders and leukodystrophy. With the development of targeted therapies, there is an urgent unmet need for validated tools...
4.
Amedick L, Martin P, Beschle J, Strolin M, Wilke M, Wolf N, et al.
Neuropediatrics
. 2023 Apr;
54(4):244-252.
PMID: 37054976
Background: Metachromatic leukodystrophy (MLD) is a lysosomal enzyme deficiency disorder leading to progressive demyelination and, consecutively, to cognitive and motor decline. Brain magnetic resonance imaging (MRI) can detect affected white...
5.
Passos L, Terraciano P, Wolf N, Oliveira F, Almeida I, Passos E
Rev Bras Ginecol Obstet
. 2022 May;
44(6):614-620.
PMID: 35576969
The impact of (CT) infection on female's fertility is not completely established yet, since the level of evidence associating these factors is still weak. Hence, the goal of the present...
6.
Elgun S, Waibel J, Kehrer C, van Rappard D, Bohringer J, Beck-Wodl S, et al.
Orphanet J Rare Dis
. 2019 Jun;
14(1):136.
PMID: 31186049
Background: Metachromatic Leukodystrophy (MLD) is a rare autosomal-recessive lysosomal storage disorder caused by mutations in the ARSA gene. While interventional trials often use untreated siblings as controls, the genotype-phenotype correlation...
7.
Van Haren K, Engelen M, Wolf N
Neurology
. 2019 Mar;
92(15):691-693.
PMID: 30902909
No abstract available.
8.
9.
Plecko B, Paul K, Mills P, Clayton P, Paschke E, Maier O, et al.
Neurology
. 2014 Mar;
82(16):1425-33.
PMID: 24658933
Objective: To determine whether patients with pyridoxine-responsive seizures but normal biomarkers for antiquitin deficiency and normal sequencing of the ALDH7A1 gene may have PNPO mutations. Methods: We sequenced the PNPO...
10.
van der Lei H, Steenweg M, Barkhof F, de Grauw T, DHooghe M, Morton R, et al.
Neuropediatrics
. 2012 Mar;
43(1):22-6.
PMID: 22430157
Objective: MRI in vanishing white matter typically shows diffuse abnormality of the cerebral white matter, which becomes increasingly rarefied and cystic. We investigated the MRI characteristics preceding this stage. Design:...