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Systematic review with meta‐analysis: Lactobacillus rhamnosus GG for treating acute gastroenteritis in children – a 2019 update

Alimentary pharmacology & therapeutics, 2019-06, Vol.49 (11), p.1376-1384

2019

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Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement

Nature reviews. Endocrinology, 2018-04, Vol.14 (4), p.229-249

2018

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The risk factors of ketoacidosis in children with newly diagnosed type 1 diabetes mellitus

Pediatric diabetes, 2011-06, Vol.12 (4pt1), p.302-306

2011

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Housing Expectations of Future Seniors Based on an Example of the Inhabitants of Poland

Buildings (Basel), 2021-07, Vol.11 (7), p.305

2021

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Infant formulae supplemented with prebiotics: Are they better than unsupplemented formulae? An updated systematic review

British journal of nutrition, 2018-04, Vol.119 (7), p.810-825

2018

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No Effect of Proton Pump Inhibitors on Crying and Irritability in Infants: Systematic Review of Randomized Controlled Trials

The Journal of pediatrics, 2015-03, Vol.166 (3), p.767-770.e3

2015

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Fermented infant formulas without live bacteria: a systematic review

European Journal of Pediatrics, 2015-11, Vol.174 (11), p.1413-1420

2015

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Early Life Exposure to Antibiotics and Autism Spectrum Disorders: A Systematic Review

Journal of autism and developmental disorders, 2019-09, Vol.49 (9), p.3866-3876

2019

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Overuse continues despite no new evidence on the efficacy of proton pump inhibitors for crying and irritability in infants

Acta Paediatrica, 2022-03, Vol.111 (3), p.682-683

2022

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Association between early life (prenatal and postnatal) antibiotic administration and coeliac disease: a systematic review

Archives of disease in childhood, 2019-11, Vol.104 (11), p.1083-1089

2019

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Postlingual hearing loss as a mitochondrial 3243A>G mutation phenotype

PloS one, 2012-10, Vol.7 (10), p.e44054-e44054

2012

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Effects of Prenatal and/or Postnatal (Maternal and/or Child) Folic Acid Supplementation on the Mental Performance of Children

Critical reviews in food science and nutrition, 2012-11, Vol.52 (11), p.959-964

2012

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A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith–Wiedemann or Silver–Russell syndrome in a single family

American journal of medical genetics. Part A, 2017-01, Vol.173 (1), p.72-78

2017

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Lymphoid tyrosine phosphatase (PTPN22/LYP) variant and Graves' disease in a Polish population: association and gene dose-dependent correlation with age of onset

Clinical endocrinology (Oxford), 2005-06, Vol.62 (6), p.679-682

2005

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M34T and V37I mutations in GJB2 associated hearing impairment: Evidence for pathogenicity and reduced penetrance

American journal of medical genetics. Part A, 2007-11, Vol.143A (21), p.2534-2543

2007

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Novel pathogenic variant in the HRAS gene with lethal outcome and a broad phenotypic spectrum among Polish patients with Costello syndrome

Clinical dysmorphology, 2017-04, Vol.26 (2), p.83-90

2017

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Is diagnosing cardio-facio-cutaneous (CFC) syndrome still a challenge? Delineation of the phenotype in 15 Polish patients with proven mutations, including novel mutations in the BRAF1 gene

European journal of medical genetics, 2015-01, Vol.58 (1), p.14-20

2015

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Infant Formulas With Postbiotics

Journal of pediatric gastroenterology and nutrition, 2022-06, Vol.74 (6), p.823-829

2022

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Recombinant growth hormone therapy in a girl with Costello syndrome: a 4-year observation

Italian journal of pediatrics, 2016-01, Vol.42 (1), p.10-10, Article 10

2016

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Sustained metabolic control and low rates of severe hypoglycaemic episodes in preschool diabetic children treated with continuous subcutaneous insulin infusion

Acta Paediatrica, 2007-06, Vol.96 (6), p.881-884

2007

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Infant Formulas With Postbiotics: An Updated Systematic Review

Journal of pediatric gastroenterology and nutrition, 2022-06, Vol.74 (6), p.823-829

2022

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Ectopic virilising adrenocortical tumour in the spinal region in an 8 year-old boy: a case report and review of the literature

Italian journal of pediatrics, 2015-09, Vol.41 (1), p.62-62, Article 62

2015

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A girl with two syndromes: Turner syndrome and Costello syndrome. A case history

American journal of medical genetics. Part A, 2012-06, Vol.158A (6), p.1486-1488

2012

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Rare clinical findings in three sporadic cases of Beckwith-Wiedemann syndrome due to novel mutations in the CDKN1C gene

Clinical dysmorphology, 2020-01, Vol.29 (1), p.28-34

2020

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Systematic review with meta‐analysis: Lactobacillus rhamnosus GG for treating acute gastroenteritis in children – a 2019 update

Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement

The risk factors of ketoacidosis in children with newly diagnosed type 1 diabetes mellitus

Housing Expectations of Future Seniors Based on an Example of the Inhabitants of Poland

Infant formulae supplemented with prebiotics: Are they better than unsupplemented formulae? An updated systematic review

No Effect of Proton Pump Inhibitors on Crying and Irritability in Infants: Systematic Review of Randomized Controlled Trials

Fermented infant formulas without live bacteria: a systematic review

Early Life Exposure to Antibiotics and Autism Spectrum Disorders: A Systematic Review

Overuse continues despite no new evidence on the efficacy of proton pump inhibitors for crying and irritability in infants

Association between early life (prenatal and postnatal) antibiotic administration and coeliac disease: a systematic review

Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to EFNA5, BAHD1 and PPP2R5E as novel candidates for genes causing human Mendelian disorders

Postlingual hearing loss as a mitochondrial 3243A>G mutation phenotype

Effects of Prenatal and/or Postnatal (Maternal and/or Child) Folic Acid Supplementation on the Mental Performance of Children

A novel IGF2/H19 domain triplication in the 11p15.5 imprinting region causing either Beckwith–Wiedemann or Silver–Russell syndrome in a single family

Lymphoid tyrosine phosphatase (PTPN22/LYP) variant and Graves' disease in a Polish population: association and gene dose-dependent correlation with age of onset

M34T and V37I mutations in GJB2 associated hearing impairment: Evidence for pathogenicity and reduced penetrance

Novel pathogenic variant in the HRAS gene with lethal outcome and a broad phenotypic spectrum among Polish patients with Costello syndrome

Is diagnosing cardio-facio-cutaneous (CFC) syndrome still a challenge? Delineation of the phenotype in 15 Polish patients with proven mutations, including novel mutations in the BRAF1 gene

Infant Formulas With Postbiotics

Recombinant growth hormone therapy in a girl with Costello syndrome: a 4-year observation

Sustained metabolic control and low rates of severe hypoglycaemic episodes in preschool diabetic children treated with continuous subcutaneous insulin infusion

Infant Formulas With Postbiotics: An Updated Systematic Review

Ectopic virilising adrenocortical tumour in the spinal region in an 8 year-old boy: a case report and review of the literature

A girl with two syndromes: Turner syndrome and Costello syndrome. A case history

Rare clinical findings in three sporadic cases of Beckwith-Wiedemann syndrome due to novel mutations in the CDKN1C gene

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