H P H Kremer
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Explore the profile of H P H Kremer including associated specialties, affiliations and a list of published articles.
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Articles
32
Citations
562
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Recent Articles
1.
[The value of re-evaluation and thorough family history taking for the diagnostic work-up of chorea]
Luykx J, van Duijn E, Geerdinck B, Burgers E, Kremer H, Veenhuizen R
Tijdschr Psychiatr
. 2024 Feb;
66(1):51-54.
PMID: 38380489
The differential diagnosis of chorea encompasses a broad range of disorders. In psychiatry, tardive dyskinesia may be difficult to discern from other causes, particularly when the family history is negative....
2.
Brandsma R, Verschuuren-Bemelmans C, Amrom D, Barisic N, Baxter P, Bertini E, et al.
Eur J Paediatr Neurol
. 2019 Sep;
23(5):692-706.
PMID: 31481303
Early onset cerebellar Ataxia (EOAc) comprises a large group of rare heterogeneous disorders. Determination of the underlying etiology can be difficult given the broad differential diagnosis and the complexity of...
3.
Uittenbroek R, Kremer H, Spoorenberg S, Reijneveld S, Wynia K
Ned Tijdschr Geneeskd
. 2017 Jun;
161:D1141.
PMID: 28659201
Objective: To examine the impact of Embrace (Dutch: SamenOud), a new primary care model for community-living people aged over 75 years on perceived quality of care. Design: Randomized controlled trial...
4.
de Bot S, Veldink J, Vermeer S, Mensenkamp A, Brugman F, Scheffer H, et al.
J Neurol
. 2012 Oct;
260(3):869-75.
PMID: 23108492
SPAST mutations are the most common cause of autosomal dominant hereditary spastic paraplegias (AD-HSPs), but many spastic paraplegia patients are found to carry no mutations in this gene. In order...
5.
van Gassen K, van der Heijden C, de Bot S, den Dunnen W, van den Berg L, Verschuuren-Bemelmans C, et al.
Brain
. 2012 Sep;
135(Pt 10):2994-3004.
PMID: 22964162
Spastic paraplegia type 7 is an autosomal recessive neurodegenerative disorder mainly characterized by progressive bilateral lower limb spasticity and referred to as a form of hereditary spastic paraplegia. Additional disease...
6.
de Bot S, van de Warrenburg B, Kremer H, Willemsen M
Neurology
. 2010 Nov;
75(19):e75-9.
PMID: 21060088
No abstract available.
7.
de Hosson L, van de Warrenburg B, Preijers F, Blijlevens N, van der Reijden B, Kremer H, et al.
Bone Marrow Transplant
. 2010 Nov;
46(8):1071-6.
PMID: 21042305
Five patients with adult-onset metachromatic leukodystrophy (MLD) underwent allo-SCT. Conditioning was reduced in intensity and grafts were obtained from voluntary unrelated donors. All but one graft were depleted of T-lymphocytes....
8.
de Bot S, van den Elzen R, Mensenkamp A, Schelhaas H, Willemsen M, Knoers N, et al.
J Neurol Neurosurg Psychiatry
. 2010 Jun;
81(10):1073-8.
PMID: 20562464
Background: In the clinically and genetically heterogeneous group of the hereditary spastic paraplegias (HSPs), mutations in the SPAST gene are most frequently found and cause a pure autosomal dominant form....
9.
Verhagen M, Abdo W, Willemsen M, Hogervorst F, Smeets D, Hiel J, et al.
Neurology
. 2009 Jun;
73(6):430-7.
PMID: 19535770
Objective: To describe the phenotype of adult patients with variant and classic ataxia-telangiectasia (A-T), to raise the degree of clinical suspicion for the diagnosis variant A-T, and to assess a...
10.
de Bot S, Kremer H, Dooijes D, Verbeek M
J Alzheimers Dis
. 2009 Jun;
17(1):53-7.
PMID: 19494431
In sporadic Alzheimer's disease (AD), cerebrospinal fluid (CSF) analysis is becoming increasingly relevant to establish an early diagnosis. We present a case of familial AD due to a presenilin-1 mutation...