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Items: 1 to 50 of 152

1.

Triclofos Sodium for Pediatric Sedation in Non-Painful Neurodiagnostic Studies.

Kaplan E, Daka A, Weissbach A, Kraus D, Kadmon G, Milkh R, Nahum E.

Paediatr Drugs. 2019 Jul 11. doi: 10.1007/s40272-019-00346-6. [Epub ahead of print]

PMID:
31292919
2.

The author replies.

Weissbach A.

Pediatr Crit Care Med. 2019 Jun;20(6):591. doi: 10.1097/PCC.0000000000001952. No abstract available.

PMID:
31162364
3.

The author replies.

Weissbach A.

Pediatr Crit Care Med. 2019 Jun;20(6):589-590. doi: 10.1097/PCC.0000000000001951. No abstract available.

PMID:
31162362
4.

The Hemodynamic Effect of Intravenous Paracetamol in Children: A Retrospective Chart Review.

Nahum E, Friedman M, Kaplan E, Weissbach A, Kadmon G.

Paediatr Drugs. 2019 Jun;21(3):177-183. doi: 10.1007/s40272-019-00336-8.

PMID:
31155693
5.

Somatosensory-motor cortex interactions measured using dual-site transcranial magnetic stimulation.

Brown MJN, Weissbach A, Pauly MG, Vesia M, Gunraj C, Baarbé J, Münchau A, Bäumer T, Chen R.

Brain Stimul. 2019 Apr 23. pii: S1935-861X(19)30200-1. doi: 10.1016/j.brs.2019.04.009. [Epub ahead of print]

PMID:
31043330
6.

Prevalence of acute kidney injury after liver transplantation in children: Comparison of the pRIFLE, AKIN, and KDIGO criteria using corrected serum creatinine.

Nahum E, Kadmon G, Kaplan E, Weissbach A, Hijazi H, Haskin O, Mozer-Glassberg Y.

J Crit Care. 2019 Apr;50:275-279. doi: 10.1016/j.jcrc.2019.01.010. Epub 2019 Jan 14.

PMID:
30665180
7.

Association of Pallidal Neurostimulation and Outcome Predictors With X-linked Dystonia Parkinsonism.

Brüggemann N, Domingo A, Rasche D, Moll CKE, Rosales RL, Jamora RDG, Hanssen H, Münchau A, Graf J, Weissbach A, Tadic V, Diesta CC, Volkmann J, Kühn A, Münte TF, Tronnier V, Klein C.

JAMA Neurol. 2019 Feb 1;76(2):211-216. doi: 10.1001/jamaneurol.2018.3777.

PMID:
30508028
8.

Acute Kidney Injury in Critically Ill Children Admitted to the PICU for Diabetic Ketoacidosis. A Retrospective Study.

Weissbach A, Zur N, Kaplan E, Kadmon G, Gendler Y, Nahum E.

Pediatr Crit Care Med. 2019 Jan;20(1):e10-e14. doi: 10.1097/PCC.0000000000001758.

PMID:
30358661
9.

Predictors of alcohol responsiveness in dystonia.

Junker J, Brandt V, Berman BD, Vidailhet M, Roze E, Weissbach A, Comella C, Malaty IA, Jankovic J, LeDoux MS, Berardelli A, Barbano R, Reich SG, Perlmutter JS, Jinnah HA, Brüggemann N.

Neurology. 2018 Nov 20;91(21):e2020-e2026. doi: 10.1212/WNL.0000000000006551. Epub 2018 Oct 19.

PMID:
30341158
10.

Associative plasticity in supplementary motor area - motor cortex pathways in Tourette syndrome.

Tübing J, Gigla B, Brandt VC, Verrel J, Weissbach A, Beste C, Münchau A, Bäumer T.

Sci Rep. 2018 Aug 10;8(1):11984. doi: 10.1038/s41598-018-30504-8.

11.

The potential for dispersal of microalgal resting cysts by migratory birds.

Tesson SVM, Weißbach A, Kremp A, Lindström Å, Rengefors K.

J Phycol. 2018 Aug;54(4):518-528. doi: 10.1111/jpy.12756. Epub 2018 Jul 10.

PMID:
29889985
12.

Pregnancy management and outcome in patients with four different tetrahydrobiopterin disorders.

Kuseyri O, Weissbach A, Bruggemann N, Klein C, Giżewska M, Karall D, Scholl-Bürgi S, Romanowska H, Krzywińska-Zdeb E, Monavari AA, Knerr I, Yapıcı Z, Leuzzi V, Opladen T.

J Inherit Metab Dis. 2018 Sep;41(5):849-863. doi: 10.1007/s10545-018-0169-0. Epub 2018 Mar 28.

PMID:
29594647
13.

Case Not Closed: Prescription Errors 12 Years after Computerized Physician Order Entry Implementation.

Kadmon G, Pinchover M, Weissbach A, Kogan Hazan S, Nahum E.

J Pediatr. 2017 Nov;190:236-240.e2. doi: 10.1016/j.jpeds.2017.08.013.

PMID:
29144250
14.

Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias.

Hebert E, Borngräber F, Schmidt A, Rakovic A, Brænne I, Weissbach A, Hampf J, Vollstedt EJ, Größer L, Schaake S, Müller M, Manzoor H, Jabusch HC, Alvarez-Fischer D, Kasten M, Kostic VS, Gasser T, Zeuner KE, Kim HJ, Jeon B, Bauer P, Altenmüller E, Klein C, Lohmann K.

Genes (Basel). 2017 Oct 18;8(10). pii: E276. doi: 10.3390/genes8100276. Review.

15.

Alcohol improves cerebellar learning deficit in myoclonus-dystonia: A clinical and electrophysiological investigation.

Weissbach A, Werner E, Bally JF, Tunc S, Löns S, Timmann D, Zeuner KE, Tadic V, Brüggemann N, Lang A, Klein C, Münchau A, Bäumer T.

Ann Neurol. 2017 Oct;82(4):543-553. doi: 10.1002/ana.25035. Epub 2017 Sep 25.

PMID:
28869676
16.

Influence of L-dopa on subtle motor signs in heterozygous Parkin- and PINK1 mutation carriers.

Weissbach A, König IR, Hückelheim K, Pramstaller PP, Werner E, Brüggemann N, Tadic V, Lohmann K, Bäumer T, Münchau A, Kasten M, Klein C.

Parkinsonism Relat Disord. 2017 Sep;42:95-99. doi: 10.1016/j.parkreldis.2017.07.003. Epub 2017 Jul 8.

PMID:
28716427
17.

Serum Tumor Necrosis Factor-Alpha Levels in Children with Nephrotic Syndrome: A Pilot Study.

Weissbach A, Garty BZ, Lagovsky I, Krause I, Davidovits M.

Isr Med Assoc J. 2017 Jan;19(1):30-33.

18.

Faithful SGCE imprinting in iPSC-derived cortical neurons: an endogenous cellular model of myoclonus-dystonia.

Grütz K, Seibler P, Weissbach A, Lohmann K, Carlisle FA, Blake DJ, Westenberger A, Klein C, Grünewald A.

Sci Rep. 2017 Feb 3;7:41156. doi: 10.1038/srep41156.

19.

Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5-Mutation-Associated Disease: A Report of Two Cases.

Westenberger A, Max C, Brüggemann N, Domingo A, Grütz K, Pawlack H, Weissbach A, Kühn AA, Spiegler J, Lang AE, Sperner J, Fung VSC, Schallner J, Gillessen-Kaesbach G, Münchau A, Klein C.

J Pediatr. 2017 Feb;181:306-308.e1. doi: 10.1016/j.jpeds.2016.10.079. Epub 2016 Dec 6.

PMID:
27931826
20.

Abnormal premotor-motor interaction in heterozygous Parkin- and Pink1 mutation carriers.

Weissbach A, Bäumer T, Pramstaller PP, Brüggemann N, Tadic V, Chen R, Klein C, Münchau A.

Clin Neurophysiol. 2017 Jan;128(1):275-280. doi: 10.1016/j.clinph.2016.10.007. Epub 2016 Oct 26.

PMID:
27843055
21.

Clinical and genetic features of cervical dystonia in a large multicenter cohort.

LeDoux MS, Vemula SR, Xiao J, Thompson MM, Perlmutter JS, Wright LJ, Jinnah HA, Rosen AR, Hedera P, Comella CL, Weissbach A, Junker J, Jankovic J, Barbano RL, Reich SG, Rodriguez RL, Berman BD, Chouinard S, Severt L, Agarwal P, Stover NP.

Neurol Genet. 2016 Apr 11;2(3):e69. doi: 10.1212/NXG.0000000000000069. eCollection 2016 Jun.

22.

A nonsense mutation in CHCHD2 in a patient with Parkinson disease.

Koschmidder E, Weissbach A, Brüggemann N, Kasten M, Klein C, Lohmann K.

Neurology. 2016 Feb 9;86(6):577-9. doi: 10.1212/WNL.0000000000002361. Epub 2016 Jan 13. No abstract available.

PMID:
26764027
23.

Premotor-motor excitability is altered in dopa-responsive dystonia.

Weissbach A, Bäumer T, Brüggemann N, Tadic V, Zittel S, Cheng B, Thomalla G, Klein C, Münchau A.

Mov Disord. 2015 Oct;30(12):1705-9. doi: 10.1002/mds.26365. Epub 2015 Jul 31.

PMID:
26230973
24.

The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort.

Mencacci NE, R'bibo L, Bandres-Ciga S, Carecchio M, Zorzi G, Nardocci N, Garavaglia B, Batla A, Bhatia KP, Pittman AM, Hardy J, Weissbach A, Klein C, Gasser T, Lohmann E, Wood NW.

Hum Mol Genet. 2015 Sep 15;24(18):5326-9. doi: 10.1093/hmg/ddv255. Epub 2015 Jul 8.

25.

A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia.

Mencacci NE, Rubio-Agusti I, Zdebik A, Asmus F, Ludtmann MH, Ryten M, Plagnol V, Hauser AK, Bandres-Ciga S, Bettencourt C, Forabosco P, Hughes D, Soutar MM, Peall K, Morris HR, Trabzuni D, Tekman M, Stanescu HC, Kleta R, Carecchio M, Zorzi G, Nardocci N, Garavaglia B, Lohmann E, Weissbach A, Klein C, Hardy J, Pittman AM, Foltynie T, Abramov AY, Gasser T, Bhatia KP, Wood NW.

Am J Hum Genet. 2015 Jun 4;96(6):938-47. doi: 10.1016/j.ajhg.2015.04.008. Epub 2015 May 14.

26.

Neurophysiological fingerprints of X-linked dystonia-parkinsonism: A model basal ganglia disease.

Weissbach A, Bäumer T, Rosales R, Lee LV, Brüggemann N, Domingo A, Westenberger A, Jamora RD, Diesta CC, Brandt V, Tadic V, Zittel S, Klein C, Münchau A.

Mov Disord. 2015 May;30(6):873-5. doi: 10.1002/mds.26224. Epub 2015 Apr 25. No abstract available.

PMID:
25914216
27.

Accumulation of rare variants in the arylsulfatase G (ARSG) gene in task-specific dystonia.

Nibbeling E, Schaake S, Tijssen MA, Weissbach A, Groen JL, Altenmüller E, Verbeek DS, Lohmann K.

J Neurol. 2015 May;262(5):1340-3. doi: 10.1007/s00415-015-7718-3. Epub 2015 Apr 1.

PMID:
25825126
28.

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.

Theuns J, Verstraeten A, Sleegers K, Wauters E, Gijselinck I, Smolders S, Crosiers D, Corsmit E, Elinck E, Sharma M, Krüger R, Lesage S, Brice A, Chung SJ, Kim MJ, Kim YJ, Ross OA, Wszolek ZK, Rogaeva E, Xi Z, Lang AE, Klein C, Weissbach A, Mellick GD, Silburn PA, Hadjigeorgiou GM, Dardiotis E, Hattori N, Ogaki K, Tan EK, Zhao Y, Aasly J, Valente EM, Petrucci S, Annesi G, Quattrone A, Ferrarese C, Brighina L, Deutschländer A, Puschmann A, Nilsson C, Garraux G, LeDoux MS, Pfeiffer RF, Boczarska-Jedynak M, Opala G, Maraganore DM, Engelborghs S, De Deyn PP, Cras P, Cruts M, Van Broeckhoven C; GEO-PD Consortium.

Neurology. 2014 Nov 18;83(21):1906-13. doi: 10.1212/WNL.0000000000001012. Epub 2014 Oct 17.

29.

Hereditary dystonia and parkinsonism: two sides of the same coin?

Weissbach A, Klein C.

Brain. 2014 Sep;137(Pt 9):2402-4. doi: 10.1093/brain/awu181. No abstract available.

PMID:
25125585
30.

Unraveling cellular phenotypes of novel TorsinA/TOR1A mutations.

Vulinovic F, Lohmann K, Rakovic A, Capetian P, Alvarez-Fischer D, Schmidt A, Weißbach A, Erogullari A, Kaiser FJ, Wiegers K, Ferbert A, Rolfs A, Klein C, Seibler P.

Hum Mutat. 2014 Sep;35(9):1114-22. doi: 10.1002/humu.22604. Epub 2014 Jul 17.

PMID:
24931141
31.

[Eyelid swelling of unclear genesis].

Weißbach A, Herberhold S, Wenzel J, Löffler KU.

Ophthalmologe. 2014 Jan;111(1):65-8. doi: 10.1007/s00347-013-2925-8. German. No abstract available.

PMID:
23996064
32.

[Dacryocystorhinostomy as part of the interdisciplinary treatment of lacrimal duct].

Herberhold S, Lindner R, Wilhelm K, Kühnemund M, Schröck A, Jakob M, Förl M, Domeier E, Mäueler TJ, Bedar MS, Keiner S, Weißbach A.

HNO. 2013 Oct;61(10):851-8. doi: 10.1007/s00106-013-2672-9. German.

PMID:
23483245
33.

Prominent psychiatric comorbidity in the dominantly inherited movement disorder myoclonus-dystonia.

Weissbach A, Kasten M, Grünewald A, Brüggemann N, Trillenberg P, Klein C, Hagenah J.

Parkinsonism Relat Disord. 2013 Apr;19(4):422-5. doi: 10.1016/j.parkreldis.2012.12.004. Epub 2013 Jan 15.

PMID:
23332219
34.

Exome sequencing in a family with restless legs syndrome.

Weissbach A, Siegesmund K, Brüggemann N, Schmidt A, Kasten M, Pichler I, Muhle H, Lohmann E, Lohnau T, Schwinger E, Hagenah J, Stephani U, Pramstaller PP, Klein C, Lohmann K.

Mov Disord. 2012 Nov;27(13):1686-9. doi: 10.1002/mds.25191.

PMID:
23192925
35.

Frequency of the D620N mutation in VPS35 in Parkinson disease.

Kumar KR, Weissbach A, Heldmann M, Kasten M, Tunc S, Sue CM, Svetel M, Kostić VS, Segura-Aguilar J, Ramirez A, Simon DK, Vieregge P, Münte TF, Hagenah J, Klein C, Lohmann K.

Arch Neurol. 2012 Oct;69(10):1360-4.

PMID:
22801713
36.

Respiratory alkalosis and metabolic acidosis in a child treated with sulthiame.

Weissbach A, Tirosh I, Scheuerman O, Hoffer V, Garty BZ.

Pediatr Emerg Care. 2010 Oct;26(10):752-3. doi: 10.1097/PEC.0b013e3181f39b4b.

PMID:
20930598
37.

Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15.

Weissbach A, Djarmati A, Klein C, Dragasević N, Zühlke C, Raković A, Guzvić M, Butz E, Tönnies H, Siebert R, Petrović I, Svetel M, Kostić VS, Lohmann K.

Mov Disord. 2010 Aug 15;25(11):1577-82. doi: 10.1002/mds.22857.

PMID:
20589871
38.

[Glued eyelids by cyanoacrylate glue (superglue)].

Lammersdorf K, Weissbach A, Meyer CH.

Klin Monbl Augenheilkd. 2010 Feb;227(2):149-50. doi: 10.1055/s-0028-1109764. Epub 2010 Feb 12. German. No abstract available.

PMID:
20155658
39.

Adenotonsilectomy improves enuresis in children with obstructive sleep apnea syndrome.

Weissbach A, Leiberman A, Tarasiuk A, Goldbart A, Tal A.

Int J Pediatr Otorhinolaryngol. 2006 Aug;70(8):1351-6. Epub 2006 Feb 28.

PMID:
16504310
40.

A chronicle of DNA methylation (1948-1975).

Weissbach A.

EXS. 1993;64:1-10. Review. No abstract available.

PMID:
8418945
41.

Organellar DNA replication in Nicotiana tabacum cultured cells.

Infante D, Weissbach A.

Plant Mol Biol. 1990 Jun;14(6):891-7.

PMID:
2102874
42.

Chloroplast and mitochondrial DNA polymerases from cultured soybean cells.

Heinhorst S, Cannon GC, Weissbach A.

Plant Physiol. 1990 Apr;92(4):939-45.

43.
44.

An Examination of the Plastid DNA of Hypohaploid Nicotiana plumbaginifolia Plants.

Cannon GC, Van KT, Heinhorst S, Trinh TH, Weissbach A.

Plant Physiol. 1989 Jun;90(2):390-3.

45.

Eukaryotic DNA methylation and gene expression.

Weissbach A, Ward C, Bolden A.

Curr Top Cell Regul. 1989;30:1-21. Review. No abstract available.

PMID:
2695289
46.

Eukaryotic DNA methylation and demethylation--sequence and strand specificity.

Weissbach A.

Bioessays. 1987 Dec;7(6):273-4. Review. No abstract available.

PMID:
3325056
47.

In vitro methylation of the 5'-flanking regions of the mouse beta-globin gene.

Ward C, Bolden A, Nalin CM, Weissbach A.

J Biol Chem. 1987 Aug 15;262(23):11057-63.

48.

[Microinvasive stage Ia cancer of the uterine cervix--a population based analysis].

Ebeling K, Weissbach A, Nischan P.

Zentralbl Gynakol. 1987;109(10):634-46. German.

PMID:
3617984
49.

[Determination of estriol in the serum of pregnant patients with a homogeneous enzyme immunoassay].

Hofmann F, Hofmann L, Weissbach A, Hubl W, Meissner D, Thiele HJ.

Z Med Lab Diagn. 1987;28(3):143-51. German. No abstract available.

PMID:
3300068

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