[Rare vascular diseases of the brain stem. The "locked-in" syndrome]

Arginine and tetrahydrobiopterin supplementation in rats with salt-induced blood pressure increase: minor hypotensive effect but improvement of renal haemodynamics.

Journal of physiology and pharmacology : an official journal of the Polish Physiological Society·2019

Changing phenotypic expression in a patient with a mitochondrial encephalopathy due to 13042G>A de novo mutation--a 5 year follow up.

Metabolic brain disease·2015

Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patients.

Neurologia i neurochirurgia polska·2013

Late onset GM2 gangliosidosis mimicking spinal muscular atrophy.

Gene·2013

Muscle pathology in myotonic dystrophy: light and electron microscopic investigation in eighteen patients.

Folia morphologica·2011

Evaluation of matrix metalloproteinases in serum of patients with amyotrophic lateral sclerosis with pattern recognition methods.

Journal of physiology and pharmacology : an official journal of the Polish Physiological Society·2010

Cerebral infarcts in newborns and infants with cyanotic cardiac anomalies.

Neuropatologia polska·1993

Effect of clinical death on inositol 1,4,5-trisphosphate in the rat brain.

Neuropatologia polska·1993

Intravascular coagulation in the central nervous system in patients with acute myeloblastic leukemias.

Neuropatologia polska·1993

Paraneoplastic subacute sensory neuronopathy. Clinical-pathological study.

Neuropatologia polska·1993

Morphological changes in the peripheral nervous system in the case of congenital malformations of the spinal cord.

Neuropatologia polska·1993

Rare coexistence of congenital malformations in adult.

Neuropatologia polska·1993

Phenotypic and Genotypic Analysis of Two Rare Cases of --SEA/-α4.3 HbH Disease.

Journal of clinical laboratory analysis·2026

Unusual Vascular Claudication in a Seronegative Patient: Raynaud's Phenomenon or Atypical Buerger Disease.

Cureus·2026

Papillary fibroelastoma of the coumadin ridge as an unusual cause of recurrent ischemic stroke: a case report.

The international journal of cardiovascular imaging·2026

GVHD-Associated Angiomatosis: An Overlooked Vascular Sequela of Chronic Graft-Versus-Host Disease.

Journal of cutaneous pathology·2026

Rouleaux mimicking anti-H in molecularly confirmed para-Bombay siblings: a diagnostic pitfall.

Immunohematology·2026

D-- phenotype and anti-Rh17 alloimmunization: a comprehensive review of identification and clinical management.

Immunohematology·2026

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[Rare vascular diseases of the brain stem. The "locked-in" syndrome]

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Arginine and tetrahydrobiopterin supplementation in rats with salt-induced blood pressure increase: minor hypotensive effect but improvement of renal haemodynamics.

Changing phenotypic expression in a patient with a mitochondrial encephalopathy due to 13042G>A de novo mutation--a 5 year follow up.

Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patients.

Late onset GM2 gangliosidosis mimicking spinal muscular atrophy.

Muscle pathology in myotonic dystrophy: light and electron microscopic investigation in eighteen patients.

Evaluation of matrix metalloproteinases in serum of patients with amyotrophic lateral sclerosis with pattern recognition methods.

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Effect of clinical death on inositol 1,4,5-trisphosphate in the rat brain.

Intravascular coagulation in the central nervous system in patients with acute myeloblastic leukemias.

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Morphological changes in the peripheral nervous system in the case of congenital malformations of the spinal cord.

Rare coexistence of congenital malformations in adult.

Phenotypic and Genotypic Analysis of Two Rare Cases of --SEA/-α4.3 HbH Disease.

Unusual Vascular Claudication in a Seronegative Patient: Raynaud's Phenomenon or Atypical Buerger Disease.

Papillary fibroelastoma of the coumadin ridge as an unusual cause of recurrent ischemic stroke: a case report.

GVHD-Associated Angiomatosis: An Overlooked Vascular Sequela of Chronic Graft-Versus-Host Disease.

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