C. Weiss

发表

[Primary pars plana vitrectomy. Techniques, indications, and results].

K. Bartz-Schmidt, N. Bornfeld, H. Heimann, 2008, Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft.

Scleral buckling versus primary vitrectomy in rhegmatogenous retinal detachment study (SPR Study): recruitment list evaluation. Study report no. 2

H. Heimann, S. Wolf, N. Feltgen, 2007, Graefe's Archive for Clinical and Experimental Ophthalmology.

The RELATION study: efficacy and safety of ranibizumab combined with laser photocoagulation treatment versus laser monotherapy in NPDR and PDR patients with diabetic macular oedema

P. Wiedemann, S. Liakopoulos, G. Lang, 2017, Acta ophthalmologica.

Elevation of Nepsilon-(carboxymethyl)lysine-modified advanced glycation end products in chronic liver disease is an indicator of liver cirrhosis.

M. Manns, F. Tacke, C. Trautwein, 2006, Clinical biochemistry.

Plasma fibronectin levels in acute and recovering malnourished children.

L. Sandberg, C. Weiss, M. Schleman, 1985, Clinical physiology and biochemistry.

Regionalized Pathology Correlates with Augmentation of mtDNA Copy Numbers in a Patient with Myoclonic Epilepsy with Ragged-Red Fibers (MERRF-Syndrome)

M. Schuelke, A. Brinckmann, A. von Moers, 2010, PloS one.

Clinical Efficacy and Safety of Ranibizumab Versus Dexamethasone for Central Retinal Vein Occlusion (COMRADE C): A European Label Study.

N. Eter, P. Wiedemann, S. Schmitz-Valckenberg, 2016, American journal of ophthalmology.

Treatment with Nusinersen - Challenges Regarding the Indication for Children with SMA Type 1.

A. von Moers, B. Plecko, G. Bernert, 2019, Journal of neuromuscular diseases.

Importance of Ductus venosus Doppler Assessment for Fetal Outcome in Cases of Intrauterine Growth Restriction

W. Rath, C. Weiss, S. Ritter, 2004, Fetal Diagnosis and Therapy.

Gene replacement therapy with onasemnogene abeparvovec in children with spinal muscular atrophy aged 24 months or younger and bodyweight up to 15 kg: an observational cohort study.

A. Blaschek, J. Denecke, B. Plecko, 2021, The Lancet. Child & adolescent health.

Evaluation of Metabolic Effects of Nusinersen in Patients with Spinal Muscular Atrophy

A. Kaindl, M. von der Hagen, A. Hermann, 2021, Journal of Pediatric Neurology online.

Improved upper limb function in non-ambulant children with SMA type 2 and 3 during nusinersen treatment: a prospective 3-years SMArtCARE registry study

B. Schlotter-Weigel, M. Blankenburg, P. Huppke, 2022, Orphanet Journal of Rare Diseases.

Lumbar Puncture Opening Pressure in Patients with Spinal Muscular Atrophy.

A. Tietze, A. Kaindl, C. Weiss, 2021, Neuropediatrics.

Tandem duplication of DMD exon 18 associated with epilepsy, macroglossia, and endocrinologic abnormalities

M. Schuelke, E. Klopocki, W. Kress, 2007, Muscle & nerve.

Influence of a new surface modification of intraocular lenses with fluoroalkylsilan on the adherence of endophthalmitis-causing bacteria in vitro

W. Solbach, H. Hoerauf, H. Laqua, 2006, Graefe's Archive for Clinical and Experimental Ophthalmology.

Scleral buckling versus primary vitrectomy in rhegmatogenous retinal detachment: a prospective randomized multicenter clinical study.

Ralf-Dieter Hilgers, Norbert Bornfeld, Karl Ulrich Bartz-Schmidt, 2007, Ophthalmology.

Positive effect of the combination of multilevel contracture release and glucocorticoid treatment in Duchenne muscular dystrophy

J. Funk, C. Weiss, S. Lebek, 2020, Journal of children's orthopaedics.

[Preoperative risk assessment of children with Duchenne muscular dystrophy and relevance for anesthesia and intra- and postoperative course].

C. Weiss, K. Wollinsky, H. Mehrkens, 1996, Medizinische Klinik.

Genotypic diversity and phenotypic spectrum of infantile liver failure syndrome type 1 due to variants in LARS1

J. Rosenfeld, J. Lupski, D. Horn, 2020, Genetics in Medicine.

Genotypic diversity and phenotypic spectrum of infantile liver failure syndrome type 1 due to variants in LARS1

J. Rosenfeld, J. Lupski, D. Horn, 2020, Genetics in Medicine.

New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy.

G. Comi, B. Koritnik, K. Claeys, 2020, Brain : a journal of neurology.

Mutations in RARS cause a hypomyelination disorder akin to Pelizaeus–Merzbacher disease

N. Sobreira, J. Christodoulou, C. Boehm, 2017, European Journal of Human Genetics.

Novel Therapies for Spinal Muscular Atrophy are Likely Changing the Patient Phenotype.

M. Pumberger, C. Weiss, T. Vu-Han, 2020, The spine journal : official journal of the North American Spine Society.

Optical coherence tomography on autologous translocation of choroid and retinal pigment epithelium in age-related macular degeneration

B. Kirchhof, A. Joussen, F. Heussen, 2008, Eye.

Triamcinolone versus inner-limiting membrane peeling in persistent diabetic macular edema (TIME study): design issues and implications

A. Joussen, R. Hilgers, C. Weiss, 2007, Graefe's Archive for Clinical and Experimental Ophthalmology.

Pars plana vitrectomy for diabetic macular edema. Internal limiting membrane delamination vs posterior hyaloid removal. A prospective randomized trial

H. Hammes, E. Stefánsson, H. Hoerauf, 2011, Graefe's Archive for Clinical and Experimental Ophthalmology.

Head‐to‐head comparison of ranibizumab PRN versus single‐dose dexamethasone for branch retinal vein occlusion (COMRADE‐B)

N. Eter, S. Schmitz-Valckenberg, L. Hattenbach, 2018, Acta ophthalmologica.

CARbon DIoxide for the treatment of Febrile seizures: rationale, feasibility, and design of the CARDIF-study

D. Schmitz, M. Schuelke, P. Martus, 2013, Journal of Translational Medicine.

Evaluation of Children with SMA Type 1 Under Treatment with Nusinersen within the Expanded Access Program in Germany

J. Denecke, H. Kölbel, U. Schara, 2018, Journal of neuromuscular diseases.

Newbornscreening SMA – From Pilot Project to Nationwide Screening in Germany

A. Blaschek, A. von Moers, I. Brockow, 2022, Journal of neuromuscular diseases.

Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings

Heinen, Heiko, Kehrer, 2023, medRxiv.

Effect of nusinersen on motor, respiratory and bulbar function in early-onset spinal muscular atrophy.

H. Lochmüller, D. Zöller, A. von Moers, 2022, Brain : a journal of neurology.