UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 422

Sortiert nach

Inhibition of prostaglandin synthesis reduces the induction of MyoD expression in rat soleus muscle

Journal of muscle research and cell motility, 2009-06, Vol.30 (3-4), p.139-144

2009

Volltextzugriff (PDF)

Photoacoustic Measurement of Ethane with Near-Infrared DFB Diode Laser

Journal of Spectroscopy, 2018-01, Vol.2018, p.1-5

2018

Volltextzugriff (PDF)

Autonomic neuropathy in mixed cryoglobulinemia

Journal of neurology, 2007-02, Vol.254 (2), p.215-219

2007

Volltextzugriff (PDF)

G.P.14.09 Successful flecainide therapy in paramyotonia congenita

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.646-646

2009

Volltextzugriff (PDF)

New model of marker placement to assess sagittal spine and lower limb during sit to stand: Typical kinematic pattern in LOPD

Gait & posture, 2018-10, Vol.66, p.S13-S13

2018

Volltextzugriff (PDF)

G.P.9.07 Congenital fibre type disproportion and non-compaction cardiomyopathy associated with insulin resistance

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.787-788

2008

Volltextzugriff (PDF)

Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia

Reumatismo, 2011-09, Vol.53 (1), p.26

2011

Volltextzugriff (PDF)

Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son

Journal of medical genetics, 2003-11, Vol.40 (11), p.858-863

2003

Volltextzugriff (PDF)

P.223 - Postural and gait patterns assessed by 3D movement analysis in a late onset Pompe disease sibship

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S162-S163

2017

Volltextzugriff (PDF)

Postural and gait patterns assessed by 3D movement analysis in a late onset Pompe disease sibship

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S162-S163

2017

Volltextzugriff (PDF)

C.P.1.01 Congenital fiber type disproportion and noncompaction cardiomyopathy in a patient

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.834-834

2007

Volltextzugriff (PDF)

P.445 - Calreticulin mutation in a case of myopathy

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S229-S230

2017

Volltextzugriff (PDF)

P.215 - Sensitivity and specificity of the PAS positive lymphocyte vacuoles in the diagnostic approach to late onset Pompe disease

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S160-S161

2017

Volltextzugriff (PDF)

Sensitivity and specificity of the PAS positive lymphocyte vacuoles in the diagnostic approach to late onset Pompe disease

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S160-S161

2017

Volltextzugriff (PDF)

Calreticulin mutation in a case of myopathy

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S229-S230

2017

Volltextzugriff (PDF)

Migrant health in Italy: a better health status difficult to maintain-country of origin and assimilation effects studied from the Italian risk factor surveillance data

Population health metrics, 2019-11, Vol.17 (1), p.14-11, Article 14

2019

Volltextzugriff (PDF)

Peripheral nervous system involvement in Klippel-Trenaunay syndrome

Clinical neuropathology, 2005-01, Vol.24 (1), p.42

2005

Volltextzugriff (PDF)

Musculoskeletal impairment and functional limitations in a patient affected by mutation in the laminin a-5 gene

Functional neurology, 2018-04, Vol.33 (2), p.117

2018

Volltextzugriff (PDF)

Rasagiline for sleep disorders in patients with Parkinson's disease: a prospective observational study

Neuropsychiatric disease and treatment, 2016-01, Vol.12, p.2497-2502

2016

Volltextzugriff (PDF)

Craniofacial pain followed by scalp necrosis and stroke. An unusual presentation of the primary antiphospholipid syndrome

Journal of neurology, 1999-02, Vol.246 (2), p.134-135

1999

Volltextzugriff (PDF)

Cerebral vascular anomalies in a large Italian family with late-onset glycogenosis II

BMC musculoskeletal disorders, 2013-05, Vol.14 (S2), p.P10-P10, Article P10

2013

Volltextzugriff (PDF)

Increased Cerebrospinal Fluid Levels of 3,3′,5′-Triiodothyronine in Patients with Alzheimer’s Disease

The journal of clinical endocrinology and metabolism, 2005-01, Vol.90 (1), p.198-202

2005

Volltextzugriff (PDF)

Lack of sodium channel mutation in an Italian family with paramyotonia congenita

Neurology, 1999-10, Vol.53 (7), p.1549

1999

Volltextzugriff (PDF)

The preparedness of the Italian obstetric surveillance system in the response to the emergency of the SARS-CoV-2 pandemic: methodological aspects of a population-based study

Epidemiologia e prevenzione, 2020-09, Vol.44 (5-6 Suppl 2), p.81

2020

Volltextzugriff (PDF)

A comment on: ‘Molecular diagnosis of transthyretin Met30 mutation in an Italian family with familial amyloidotic polyneuropathy’ by Paola Strocchi et al., FEBS Letters 359 (1995) 203–205

FEBS letters, 1996-11, Vol.397 (2), p.357-357

1996

Volltextzugriff (PDF)

1 – 25 von 422

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(354)
Mit Volltextzugriff
(338)

Publikationsform

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Inhibition of prostaglandin synthesis reduces the induction of MyoD expression in rat soleus muscle

Photoacoustic Measurement of Ethane with Near-Infrared DFB Diode Laser

Autonomic neuropathy in mixed cryoglobulinemia

G.P.14.09 Successful flecainide therapy in paramyotonia congenita

New model of marker placement to assess sagittal spine and lower limb during sit to stand: Typical kinematic pattern in LOPD

G.P.9.07 Congenital fibre type disproportion and non-compaction cardiomyopathy associated with insulin resistance

Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia

Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son

P.223 - Postural and gait patterns assessed by 3D movement analysis in a late onset Pompe disease sibship

Postural and gait patterns assessed by 3D movement analysis in a late onset Pompe disease sibship

C.P.1.01 Congenital fiber type disproportion and noncompaction cardiomyopathy in a patient

P.445 - Calreticulin mutation in a case of myopathy

P.215 - Sensitivity and specificity of the PAS positive lymphocyte vacuoles in the diagnostic approach to late onset Pompe disease

Sensitivity and specificity of the PAS positive lymphocyte vacuoles in the diagnostic approach to late onset Pompe disease

Calreticulin mutation in a case of myopathy

Migrant health in Italy: a better health status difficult to maintain-country of origin and assimilation effects studied from the Italian risk factor surveillance data

Peripheral nervous system involvement in Klippel-Trenaunay syndrome

Musculoskeletal impairment and functional limitations in a patient affected by mutation in the laminin a-5 gene

Rasagiline for sleep disorders in patients with Parkinson's disease: a prospective observational study

Craniofacial pain followed by scalp necrosis and stroke. An unusual presentation of the primary antiphospholipid syndrome

Cerebral vascular anomalies in a large Italian family with late-onset glycogenosis II

Increased Cerebrospinal Fluid Levels of 3,3′,5′-Triiodothyronine in Patients with Alzheimer’s Disease

Lack of sodium channel mutation in an Italian family with paramyotonia congenita

The preparedness of the Italian obstetric surveillance system in the response to the emergency of the SARS-CoV-2 pandemic: methodological aspects of a population-based study

A comment on: ‘Molecular diagnosis of transthyretin Met30 mutation in an Italian family with familial amyloidotic polyneuropathy’ by Paola Strocchi et al., FEBS Letters 359 (1995) 203–205

Suchergebnisse filtern