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Items: 34

1.

Melatonin-Measurement Methods and the Factors Modifying the Results. A Systematic Review of the Literature.

Rzepka-Migut B, Paprocka J.

Int J Environ Res Public Health. 2020 Mar 15;17(6). pii: E1916. doi: 10.3390/ijerph17061916. Review.

2.

CDKL5 Deficiency Disorder-A Complex Epileptic Encephalopathy.

Jakimiec M, Paprocka J, Śmigiel R.

Brain Sci. 2020 Feb 17;10(2). pii: E107. doi: 10.3390/brainsci10020107.

3.

Infantile Alexander Disease with Late Onset Infantile Spasms and Hypsarrhythmia.

Paprocka J, Rzepka-Migut B, Rzepka N, Jezela-Stanek A, Morava E.

Balkan J Med Genet. 2019 Dec 21;22(2):77-82. doi: 10.2478/bjmg-2019-0017. eCollection 2019 Dec.

4.

FGF12p.Gly112Ser variant as a cause of phenytoin/phenobarbital responsive epilepsy.

Paprocka J, Jezela-Stanek A, Koppolu A, Rydzanicz M, Kosińska J, Stawiński P, Płoski R.

Clin Genet. 2019 Sep;96(3):274-275. doi: 10.1111/cge.13592. Epub 2019 Jul 10.

PMID:
31292943
5.

Melatonin in Hypoxic-Ischemic Brain Injury in Term and Preterm Babies.

Paprocka J, Kijonka M, Rzepka B, Sokół M.

Int J Endocrinol. 2019 Feb 20;2019:9626715. doi: 10.1155/2019/9626715. eCollection 2019. Review.

6.

Mathematical evaluation of melatonin secretion in hypoxic ischemic encephalopathy.

Paprocka J, Kijonka M, Borys D, Emich-Widera E, Wojcieszek P, Sokół M.

Neuro Endocrinol Lett. 2018 Dec;39(5):391-400.

PMID:
30664345
7.

Megalencephalic leukoencephalopathy with subcortical cysts: Characterization of disease variants.

Hamilton EMC, Tekturk P, Cialdella F, van Rappard DF, Wolf NI, Yalcinkaya C, Çetinçelik Ü, Rajaee A, Kariminejad A, Paprocka J, Yapici Z, Bošnjak VM, van der Knaap MS; MLC Research Group.

Neurology. 2018 Apr 17;90(16):e1395-e1403. doi: 10.1212/WNL.0000000000005334. Epub 2018 Mar 21.

8.

Melatonin and Angelman Syndrome: Implications and Mathematical Model of Diurnal Secretion.

Paprocka J, Kijonka M, Wojcieszek P, Pęcka M, Emich-Widera E, Sokół M.

Int J Endocrinol. 2017;2017:5853167. doi: 10.1155/2017/5853167. Epub 2017 Dec 12.

9.

Melatonin in Tuberous Sclerosis Complex Analysis Using Modern Mathematical Modeling Methods.

Paprocka J, Kijonka M, Boguszewicz Ł, Sokół M.

Int J Endocrinol. 2017;2017:8234502. doi: 10.1155/2017/8234502. Epub 2017 Apr 25.

10.

Melatonin in Epilepsy: A New Mathematical Model of Diurnal Secretion.

Paprocka J, Kijonka M, Pęcka M, Sokół M.

Int J Endocrinol. 2016;2016:3861461. doi: 10.1155/2016/3861461. Epub 2016 Jul 13.

11.

Four-and-one-half years' experience in monitoring of reproducibility of an MR spectroscopy system--application of in vitro results to interpretation of in vivo data.

Skorupa A, Wicher M, Banasik T, Jamroz E, Paprocka J, Kiełtyka A, Sokół M, Konopka M.

J Appl Clin Med Phys. 2014 May 8;15(3):323–334. doi: 10.1120/jacmp.v15i3.4754.

12.

Magnetic resonance spectroscopy and molecular studies in ornithine transcarbamylase deficiency novel mutation c.802A>G in exon 8 (p.Met268Val).

Jamroz E, Paprocka J, Sokół M, Popowska E, Ciara E.

Neurol Neurochir Pol. 2013 May-Jun;47(3):283-9.

PMID:
23821427
13.

[Joubert syndrome and related disorders].

Paprocka J, Jamroz E.

Neurol Neurochir Pol. 2012 Jul-Aug;46(4):379-83. Review.

PMID:
23023437
14.

Hyperammonemia in children: on the crossroad of different disorders.

Paprocka J, Jamroz E.

Neurologist. 2012 Sep;18(5):261-5. doi: 10.1097/NRL.0b013e318266f58a. Review.

PMID:
22931730
15.

Isolated rhomboencephalosynapsis - a rare cerebellar anomaly.

Paprocka J, Jamroz E, Scieszka E, Kluczewska E.

Pol J Radiol. 2012 Jan;77(1):47-9.

16.

Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing.

Timal S, Hoischen A, Lehle L, Adamowicz M, Huijben K, Sykut-Cegielska J, Paprocka J, Jamroz E, van Spronsen FJ, Körner C, Gilissen C, Rodenburg RJ, Eidhof I, Van den Heuvel L, Thiel C, Wevers RA, Morava E, Veltman J, Lefeber DJ.

Hum Mol Genet. 2012 Oct 1;21(19):4151-61. doi: 10.1093/hmg/dds123. Epub 2012 Apr 5.

PMID:
22492991
17.

Clinical and neuropathological picture of ethylmalonic aciduria - diagnostic dilemma.

Jamroz E, Paprocka J, Adamek D, Pytel J, Szczechowska K, Grabska N, Malec M, Głuszkiewicz E, Daab M, Wodołażski A.

Folia Neuropathol. 2011;49(1):71-7.

18.

Melatonin and childhood refractory epilepsy--a pilot study.

Paprocka J, Dec R, Jamroz E, Marszał E.

Med Sci Monit. 2010 Sep;16(9):CR389-96.

PMID:
20802409
19.

Xp21.2 contiguous gene syndrome due to deletion involving glycerol kinase and Duchenne muscular dystrophy loci.

Jamroz E, Paprocka J, Popowska E, Pytel J, Ciara E, Adamowicz M.

Neurol India. 2010 Jul-Aug;58(4):670-1. doi: 10.4103/0028-3886.68690. No abstract available.

20.

Do children with Adams-Oliver syndrome require endocrine follow-up? New information on the phenotype and management.

Kalina MA, Kalina-Faska B, Paprocka J, Jamroz E, Pyrkosz A, Marszał E, Małecka-Tendera E.

Clin Genet. 2010 Sep;78(3):227-35. doi: 10.1111/j.1399-0004.2010.01470.x. Epub 2010 May 22.

PMID:
20560985
21.

[Sudden infant death syndrome--current opinions on etiology and pathogenesis].

Paprocka J, Jamroz E, Dyczkowski S, Marszał E.

Wiad Lek. 2009;62(2):123-8. Review. Polish.

PMID:
20141062
22.

Maternal phenylketonuria.

Paprocka J, Jamroz E, Wiktor M, Marszał E.

Wiad Lek. 2009;62(1):11-7.

PMID:
19817251
23.

[Back pain in children].

Paprocka J, Jamroz E, Głuszkiewicz E, Klimczak A, Kluczewska E, Marszał E.

Wiad Lek. 2008;61(7-9):183-9. Polish.

PMID:
19172829
24.

CDG type Ia and congenital cytomegalovirus infection: two coexisting conditions.

Jamroz E, Adamek D, Paprocka J, Adamowicz M, Marszał E, Wevers RA.

J Child Neurol. 2009 Jan;24(1):13-8. doi: 10.1177/0883073808321041.

PMID:
19168813
25.

Clinical and neuropathological picture of familial encephalopathy with bifunctional protein deficiency.

Paprocka J, Jamroz E, Adamek D, Stradomska TJ, Głuszkiewicz E, Grzybowska-Chlebowczyk U, Marszał E.

Folia Neuropathol. 2007;45(4):213-9.

26.

Angelman syndrome and hypothyroidism - coincidence or unique correlation?

Paprocka J, Jamroz E, Kalina M, Kalina-Faska B, Malecka-Tendera E, Marszal E.

Neuro Endocrinol Lett. 2007 Oct;28(5):545-6.

PMID:
17984955
27.

Angelman syndrome revisited.

Paprocka J, Jamroz E, Szwed-Białozyt B, Jezela-Stanek A, Kopyta I, Marszał E.

Neurologist. 2007 Sep;13(5):305-12.

PMID:
17848870
28.

Hereditary neuropathy with liability to pressure palsy.

Paprocka J, Kajor M, Jamroz E, Jezela-Stanek A, Seeman P, Marszał E.

Folia Neuropathol. 2006;44(4):290-4.

29.

[Niemann-Pick disease, type A: a case report].

Jamroz E, Paprocka J, Marszał E, Lugowska A, Kluczewska E.

Neurol Neurochir Pol. 2006 May-Jun;40(3):238-42. Polish.

PMID:
16794964
30.

[Neurological picture and 1H MRS in 4 children with hypoparathyroidism].

Paprocka J, Jamroz E, Wackermann-Ramos A, Sokół M, Marszał E.

Przegl Lek. 2005;62(7):680-4. Polish.

PMID:
16463701
31.

Difficulties in differentiation of Parry-Romberg syndrome, unilateral facial sclerodermia, and Rasmussen syndrome.

Paprocka J, Jamroz E, Adamek D, Marszal E, Mandera M.

Childs Nerv Syst. 2006 Apr;22(4):409-15. Epub 2005 Oct 25.

PMID:
16247619
32.

[Neurocutaneous melanosis--case report].

Paprocka J, Jamroz E, Kajor M, Marszał E.

Wiad Lek. 2004;57(9-10):520-3. Polish.

PMID:
15765773
33.

Leukoencephalopathy with macrocephaly and mild clinical course.

Marszał E, Jamroz E, Paprocka J, Kluczewska E, Sokół M.

Neurol Neurochir Pol. 2004;38(1 Suppl 1):S25-30. Erratum in: Neurol Neurochir Pol. 2004 Oct;14(4):388.

PMID:
15045864
34.

[Candidicidal activity of polymorphonuclear leukocytes in children with measles].

Pawlicka-Domańska Z, Sliwińska-Przyjemska H, Paprocka J.

Pediatr Pol. 1978 Aug;53(8):955-61. Polish. No abstract available.

PMID:
358117

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