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Healthcare resource use in myasthenia gravis: a US health claims analysis

Therapeutic advances in neurological disorders, 2023-01, Vol.16, p.17562864221150327-17562864221150327

2023

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Treatment patterns in myasthenia gravis: A United States health claims analysis

Muscle & nerve, 2023-04, Vol.67 (4), p.297-305

2023

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Using an expanded algorithm to estimate prevalence of amyotrophic lateral sclerosis in U.S. and UK

Neurological sciences, 2024-05, Vol.45 (5), p.2321-2324

2024

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The K-theory of the triple-Toeplitz deformation of the complex projective plane

Banach Center publications, 2012, Vol.98, p.303-310

Rudnik, Jan

2012

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Real-World Findings on the Characteristics and Treatment Exposures of Patients with Hidradenitis Suppurativa from US Claims Data

Dermatology and therapy, 2023-02, Vol.13 (2), p.581-594

2023

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9 Early and late clinical features in 171 patients with LGI1-antibody encephalitis

BMJ neurology open, 2023-08, Vol.5 (Suppl 1), p.A5-A5

2023

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Primary ciliary dyskinesia. From symptoms to diagnosis. A case report of a 4.5-year-old girl

Pediatria & Medycyna Rodzinna (Online), 2020-01, Vol.16 (2), p.210-216

2020

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A review of practical issues related to the diseases of the nail unit useful for doctors (including non-dermatologists)

Pediatria & Medycyna Rodzinna (Online), 2020-01, Vol.16 (1), p.62-69

2020

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L’importance de la bronchoscopie dans le traitement de l’enfant tuberculeux

Respiration, 1963, Vol.20 (5), p.275-288

1963

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Loss of tubulin deglutamylase CCP1 causes infantile‐onset neurodegeneration

The EMBO journal, 2018-12, Vol.37 (23), p.n/a

2018

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Glosa do uchwały 7 sędziów Naczelnego Sądu Administracyjnego z dnia 20 marca 2023 r., sygn. III FPS 3/22

Kwartalnik Prawa Podatkowego, 2024-03 (1), p.97-110

2024

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Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum

Orphanet journal of rare diseases, 2013-03, Vol.8 (1), p.41-41

2013

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Glosa do uchwały 7 sędziów Naczelnego Sądu Administracyjnego z dnia 20 marca 2023 r., sygn. III FPS 3/22

Kwartalnik Prawa Podatkowego, 2024 (1), p.97-110

2024

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HSJ1-related hereditary neuropathies: novel mutations and extended clinical spectrum

Neurology, 2014-11, Vol.83 (19), p.1726-1732

2014

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Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot–Marie–Tooth neuropathy type 4B2/11p15

Human molecular genetics, 2003-02, Vol.12 (3), p.349-356

2003

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Programmable half-life and anti-tumour effects of bispecific T-cell engager-albumin fusions with tuned FcRn affinity

Communications biology, 2021-03, Vol.4 (1), p.310-11, Article 310

2021

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SIL1 mutations and clinical spectrum in patients with Marinesco-Sjögren syndrome

Brain (London, England : 1878), 2013-12, Vol.136 (Pt 12), p.3634-3644

2013

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Pontocerebellar hypoplasia with spinal muscular atrophy (PCH1): identification of SLC25A46 mutations in the original Dutch PCH1 family

Brain (London, England : 1878), 2017-08, Vol.140 (8), p.e46-e46

2017

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Oligophrenin 1 (OPHN1) gene mutation causes syndromic X‐linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia

Brain (London, England : 1878), 2003-07, Vol.126 (7), p.1537-1544

2003

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Hereditary Neuropathies: Update 2017

Neuropediatrics, 2017-08, Vol.48 (4), p.282-293

2017

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Charcot-Marie-Tooth disease and hereditary motor neuropathies – Update 2020

Medizinische Genetik, 2020-10, Vol.32 (3), p.207-219

2020

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The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MME

Neurology, 2020-12, Vol.95 (24), p.e3163

2020

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Role of transcranial Doppler ultrasonography in assessing stenosis after flow diversion

Clinical neurology and neurosurgery, 2020-11, Vol.198, p.106219-106219, Article 106219

2020

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Healthcare resource use in myasthenia gravis: a US health claims analysis

Treatment patterns in myasthenia gravis: A United States health claims analysis

Using an expanded algorithm to estimate prevalence of amyotrophic lateral sclerosis in U.S. and UK

The K-theory of the triple-Toeplitz deformation of the complex projective plane

Real-World Findings on the Characteristics and Treatment Exposures of Patients with Hidradenitis Suppurativa from US Claims Data

9 Early and late clinical features in 171 patients with LGI1-antibody encephalitis

Primary ciliary dyskinesia. From symptoms to diagnosis. A case report of a 4.5-year-old girl

A review of practical issues related to the diseases of the nail unit useful for doctors (including non-dermatologists)

L’importance de la bronchoscopie dans le traitement de l’enfant tuberculeux

Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration

Loss of tubulin deglutamylase CCP1 causes infantile‐onset neurodegeneration

Glosa do uchwały 7 sędziów Naczelnego Sądu Administracyjnego z dnia 20 marca 2023 r., sygn. III FPS 3/22

Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum

Glosa do uchwały 7 sędziów Naczelnego Sądu Administracyjnego z dnia 20 marca 2023 r., sygn. III FPS 3/22

HSJ1-related hereditary neuropathies: novel mutations and extended clinical spectrum

Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot–Marie–Tooth neuropathy type 4B2/11p15

Programmable half-life and anti-tumour effects of bispecific T-cell engager-albumin fusions with tuned FcRn affinity

Pontocerebellar hypoplasia type 1: clinical spectrum and relevance of EXOSC3 mutations

SIL1 mutations and clinical spectrum in patients with Marinesco-Sjögren syndrome

Pontocerebellar hypoplasia with spinal muscular atrophy (PCH1): identification of SLC25A46 mutations in the original Dutch PCH1 family

Oligophrenin 1 (OPHN1) gene mutation causes syndromic X‐linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia

Hereditary Neuropathies: Update 2017

Charcot-Marie-Tooth disease and hereditary motor neuropathies – Update 2020

The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MME

Role of transcranial Doppler ultrasonography in assessing stenosis after flow diversion

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