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The hygienic appraisal of tables and chairs in Warsaw kindergartens

Roczniki Państwowego Zakładu Higieny, 1970, Vol.21 (1), p.101

Wieczorek-Wojeńska, W

1970

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Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients

Clinical genetics, 2016-01, Vol.89 (1), p.34-43

2016

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The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

Journal of medical genetics, 2011-06, Vol.48 (6), p.396-406

2011

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Testing alternative cascades from internalizing and externalizing symptoms to adolescent alcohol use and alcohol use disorder through co-occurring symptoms and peer delinquency

Development and psychopathology, 2021-02, Vol.33 (1), p.29-46

2021

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Mutations in SMARCB1 and in other Coffin–Siris syndrome genes lead to various brain midline defects

Nature communications, 2019-07, Vol.10 (1), p.2966-14, Article 2966

2019

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De novo variants in PAK1 lead to intellectual disability with macrocephaly and seizures

Brain (London, England : 1878), 2019-11, Vol.142 (11), p.3351-3359

2019

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Further delineation of the KAT6B molecular and phenotypic spectrum

European journal of human genetics : EJHG, 2015-09, Vol.23 (9), p.1165-1170

2015

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‘Splitting versus lumping’: Temple–Baraitser and Zimmermann–Laband Syndromes

Human genetics, 2015-10, Vol.134 (10), p.1089-1097

2015

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Haploinsufficiency of a Spliceosomal GTPase Encoded by EFTUD2 Causes Mandibulofacial Dysostosis with Microcephaly

American journal of human genetics, 2012-02, Vol.90 (2), p.369-377

2012

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Miller (Genée―Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH

Human molecular genetics, 2012-09, Vol.21 (18), p.3969-3983

2012

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De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum

Human genetics, 2015-01, Vol.134 (1), p.97-109

2015

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De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder

American journal of human genetics, 2018-06, Vol.102 (6), p.1195-1203

2018

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Phenotype and genotype in Nicolaides-Baraitser syndrome

American journal of medical genetics. Part C, Seminars in medical genetics, 2014-09, Vol.166C (3), p.302-314

2014

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Early onset systemic lupus erythematosus: differential diagnoses, clinical presentation, and treatment options

Clinical rheumatology, 2011-02, Vol.30 (2), p.275-283

2011

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FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletions

Human mutation, 2010-05, Vol.31 (5), p.E1332-E1347

2010

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Comparison of Clofarabine Activity in Childhood and Adult Acute Leukemia: Individual Tumor Response Study

Anticancer research, 2009-05, Vol.29 (5), p.1643-1650

2009

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Bohring-Opitz (Oberklaid-Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis

European journal of human genetics : EJHG, 2011-05, Vol.19 (5), p.513-519

2011

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New method for quantitative analysis of GD2 ganglioside in plasma of neuroblastoma patients

Acta biochimica Polonica, 2009-01, Vol.56 (3), p.423-431

2009

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Retroperitoneoscopic Nephrectomy in the Prone Position in Children (Point of Technique)

European urology, 2002-11, Vol.42 (5), p.516-519

2002

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Raised plasma endothelin in unstable angina and non-Q wave myocardial infarction: relation to cardiovascular outcome

British Heart Journal, 1994-11, Vol.72 (5), p.436-441

1994

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In vitro sensitivity of leukemic cells to nucleoside derivatives in childhood acute leukemias: good activity in leukemic relapses

Neoplasma, 2005, Vol.52 (1), p.74

2005

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Remaining Problems and Controversies in the Management of Childhood Head and Neck Soft Tissue Sarcomas: Retrospective (National) Multicenter Study of the Polish Pediatric Solid Tumors Group

Pediatric hematology and oncology, 2004-06, Vol.21 (4), p.349-362

2004

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Hemangioma with Kaposi's Sarcoma-Like Features: Report of two Cases

Fetal and pediatric pathology, 1989, Vol.9 (5), p.567-575

1989

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The hygienic appraisal of tables and chairs in Warsaw kindergartens

Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients

The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

Testing alternative cascades from internalizing and externalizing symptoms to adolescent alcohol use and alcohol use disorder through co-occurring symptoms and peer delinquency

Mutations in SMARCB1 and in other Coffin–Siris syndrome genes lead to various brain midline defects

De novo variants in PAK1 lead to intellectual disability with macrocephaly and seizures

Further delineation of the KAT6B molecular and phenotypic spectrum

‘Splitting versus lumping’: Temple–Baraitser and Zimmermann–Laband Syndromes

Haploinsufficiency of a Spliceosomal GTPase Encoded by EFTUD2 Causes Mandibulofacial Dysostosis with Microcephaly

Miller (Genée―Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH

De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum

De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder

Phenotype and genotype in Nicolaides-Baraitser syndrome

Early onset systemic lupus erythematosus: differential diagnoses, clinical presentation, and treatment options

FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletions

Comparison of Clofarabine Activity in Childhood and Adult Acute Leukemia: Individual Tumor Response Study

Bohring-Opitz (Oberklaid-Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis

Identification of 34 novel and 56 known FOXL2 mutations in patients with blepharophimosis syndrome

New method for quantitative analysis of GD2 ganglioside in plasma of neuroblastoma patients

Prognostic Impact of Combined Fludarabine, Treosulfan and Mitoxantrone Resistance Profile in Childhood Acute Myeloid Leukemia

Retroperitoneoscopic Nephrectomy in the Prone Position in Children (Point of Technique)

Raised plasma endothelin in unstable angina and non-Q wave myocardial infarction: relation to cardiovascular outcome

In vitro sensitivity of leukemic cells to nucleoside derivatives in childhood acute leukemias: good activity in leukemic relapses

Remaining Problems and Controversies in the Management of Childhood Head and Neck Soft Tissue Sarcomas: Retrospective (National) Multicenter Study of the Polish Pediatric Solid Tumors Group

Hemangioma with Kaposi's Sarcoma-Like Features: Report of two Cases

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