B. Lipska

发表

Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.

A. Anarat, S. Testa, G. Remuzzi, 2015, Clinical journal of the American Society of Nephrology : CJASN.

NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome

K. Tory, C. Antignac, T. Tulassay, 2013, Pediatric Nephrology.

Genotype-phenotype associations in WT1 glomerulopathy.

K. Tory, G. Caridi, P. Iatropoulos, 2014, Kidney international.

On the significance of germline cytogenetic rearrangements at MYCN locus in neuroblastoma

J. Limon, J. Wierzba, Magdalena Koczkowska, 2013, Molecular Cytogenetics.

Genetic screening in adolescents with steroid-resistant nephrotic syndrome.

A. Anarat, G. Ardissino, G. Ghiggeri, 2013, Kidney international.

Organ-sparing surgery of the bilateral testicular large cell calcifying sertoli cell tumor in patient with atypical Peutz–Jeghers syndrome

A. Pławski, K. Krajka, A. Kałużny, 2011, International Urology and Nephrology.

Serum and Urinary Cytokine Homeostasis and Renal Tubular Function in Children with Type 1 Diabetes Mellitus

J. Myśliwska, K. Zorena, A. Myśliwski, 2006, Journal of Pediatric Endocrinology & Metabolism (JPEM).

The effect of vitamin B supplementation on homocysteine metabolism and clinical state of patients with chronic epilepsy treated with carbamazepine and valproic acid

D. Ryglewicz, A. Bochyńska, A. Graban, 2012, Seizure.

Serum levels and clinical response in long-term pharmacotherapy with zuclopenthixol decanoate

K. Nurowska, B. Szukalski, B. Lipska, 2006, Psychopharmacology.

NPHS2 Mutations in Steroid‐Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum

A. Mégarbané, K. Dahan, G. Mollet, 2014, Human mutation.

Mutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian population

M. Litwin, M. Szczepańska, F. Schaefer, 2013, Journal of Applied Genetics.

Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome

M. Malinowska, J. Limon, J. Wierzba, 2013, Journal of applied genetics.

Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome

M. Malinowska, J. Limon, J. Wierzba, 2012, Journal of Applied Genetics.

On the significance of germline cytogenetic rearrangements at MYCN locus in neuroblastoma

J. Limon, J. Wierzba, Magdalena Koczkowska, 2013, Molecular Cytogenetics.

c.1810C>T Polymorphism of NTRK1Gene is associated with reduced Survival in Neuroblastoma Patients

G. Tonini, P. Scaruffi, J. Limon, 2009, BMC Cancer.

Primary leiomyosarcoma of the mesentery in two sisters: clinical and molecular characteristics.

J. Jassem, J. Limon, W. Biernat, 2013, Polish journal of pathology : official journal of the Polish Society of Pathologists.

Erratum to: Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome

M. Malinowska, J. Limon, J. Wierzba, 2013, Journal of Applied Genetics.

Mutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian population

M. Litwin, M. Szczepańska, F. Schaefer, 2013, Journal of Applied Genetics.

Predictive value of selected biochemical markers of brain damage for functional outcome in ischaemic stroke patients.

D. Ryglewicz, H. Sienkiewicz-Jarosz, A. Bidziński, 2009, Neurologia i neurochirurgia polska.