B Ryniewicz
Overview
Explore the profile of B Ryniewicz including associated specialties, affiliations and a list of published articles.
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56
Citations
106
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Recent Articles
1.
Kochanski A, Timmerman V, Jedrzejowska H, Ryniewicz B, Lofgren A, De Vriendt E, et al.
Ann N Y Acad Sci
. 2017 Nov;
883(1):493-496.
PMID: 29086975
No abstract available.
2.
Szczudlik P, Szyluk B, Lipowska M, Ryniewicz B, Kubiszewska J, Dutkiewicz M, et al.
Acta Neurol Scand
. 2014 Jun;
130(4):229-33.
PMID: 24947881
Objectives: Myasthenia gravis (MG) is an autoimmune disease caused by antibodies against neuromuscular junction proteins, 85% of patients have antibodies against acetylcholine receptor (AChR-MG). Antititin antibodies are present in a...
3.
Nadaj-Pakleza A, Dorobek M, Nestorowicz K, Ryniewicz B, Szmidt-Salkowska E, Kaminska A
Neurol Neurochir Pol
. 2013 Jul;
47(3):214-22.
PMID: 23821418
Background And Purpose: At present, more than 20 different forms of limb-girdle muscular dystrophies (LGMDs) are known (at least 7 autosomal dominant and 14 autosomal recessive). Although these different forms...
4.
Kostera-Pruszczyk A, Ryniewicz B, Rowinska-Marcinska K, Dutkiewicz M, Kaminska A
Eur J Paediatr Neurol
. 2008 Jul;
13(2):194-6.
PMID: 18585938
Lambert-Eaton myasthenic syndrome (LEMS) is a rare autoimmune disorder of the neuromuscular junction. LEMS can be associated with a variety of neoplasms. Patients present with proximal muscle weakness and fatigability,...
5.
Zielonka T, Kostera-Pruszczyk A, Ryniewicz B, Korczynski P, Szyluk B
J Physiol Pharmacol
. 2006 Oct;
57 Suppl 4:409-16.
PMID: 17072071
Myasthenia gravis (MG) is an autoimmune disorder of the neuromuscular junction. Clinical symptoms are caused by weakness and increased fatigability of various muscle groups. Myasthenia may lead to significant respiratory...
6.
Fidzianska A, Ryniewicz B, Shen X, Engel A
Neuromuscul Disord
. 2005 Oct;
15(11):753-9.
PMID: 16198106
We report a patient with a slow-channel congenital myasthenic syndrome who carries a novel slow-channel mutation in the epsilon subunit of the acetylcholine receptor and has tubulofilamentous inclusion bodies, in...
7.
Kabzinska D, Kochanski A, Drac H, Ryniewicz B, Rowinska-Marcinska K, Hausmanowa-Petrusewicz I
Neuropediatrics
. 2005 Jun;
36(3):206-9.
PMID: 15944907
A recessive demyelinating subtype of Charcot-Marie-Tooth disease called CMT4 is a heterogeneous group of disorders. A relatively frequent form of recessive CMT (CMT4 A) has been mapped to the chromosome...
8.
Fidzianska A, Kaminska A, Ryniewicz B
Neuropediatrics
. 2005 Mar;
36(1):35-9.
PMID: 15776320
We report on a 16-year-old girl with a unique neuromuscular disorder characterised by progressive proximal muscle weakness and numerous tubular aggregates, intracytoplasmic, as well as intranuclear inclusions of the IBM...
9.
Kochanski A, Kennerson M, Kawulak M, Ryniewicz B, Rowinska-Marcinska K, Walizada G, et al.
Neurology
. 2005 Feb;
64(3):533-5.
PMID: 15699389
Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2) is a heterogeneous group of disorders with seven chromosomal loci mapped in the uncomplicated forms of CMT2. The authors report clinical, electrophysiologic,...
10.
Kochanski A, Drac H, Kabzinska D, Ryniewicz B, Rowinska-Marcinska K, Nowakowski A, et al.
Neurology
. 2004 Jun;
62(11):2122-3.
PMID: 15184631
Congenital hypomyelinating neuropathy (CHN; MIM# 605253) is a severe neuropathy with early infancy onset inherited as an autosomal dominant or recessive trait. Sural nerve biopsy shows a characteristic picture of...