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Cerebral Palsy in Children as a Risk Factor for Malnutrition

Annals of nutrition and metabolism, 2015-01, Vol.66 (4), p.224-232

2015

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H2O2 and Src-dependent transactivation of the EGF receptor mediates the stimulatory effect of leptin on renal ERK and Na+, K+-ATPase

Peptides (New York, N.Y. : 1980), 2006-12, Vol.27 (12), p.3234-3244

2006

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H 2O 2 and Src-dependent transactivation of the EGF receptor mediates the stimulatory effect of leptin on renal ERK and Na +, K +-ATPase

Peptides (New York, N.Y. : 1980), 2006, Vol.27 (12), p.3234-3244

2006

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Indirect CT venography of the abdominal cavity and lower limbs in patients with the suspicion of pulmonary embolism--indications, technique, diagnostic possibilities

Annales Universitatis Mariae Curie-Skłodowska. Sectio D, Medicina, 2004, Vol.59 (2), p.508

2004

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Maple Syrup Urine Disease in a newborn infant

Medycyna wieku rozwojowego, 2007-01, Vol.11 (1), p.65

2007

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Usefulness of telemetric cardiotocography in detection of fetal compromise due to the true knot in umbilical cord

Ginekologia polska, 2024-01, Vol.95 (3), p.243-244

2024

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Management of large chronic venous leg ulcers with negative pressure wound therapy

Negative pressure wound therapy journal, 2017-12, Vol.4 (2), p.17

2017

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Erythema dyschromicum perstans (ashy dermatosis) – opis przypadków

Przegląd dermatologiczny, 2011-08, Vol.98 (4), p.322-327

2011

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2-chlorodeoxyadenosine treatment for cutaneous T-cell lymphoma

Dermatology reports, 2010-09, Vol.2 (2), p.e12-e12

2010

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Erythema dyschromicum perstans (ashy dermatosis) - case reports

Przegląd dermatologiczny, 2011-07, Vol.98 (4), p.322

2011

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Interleukin-13 promoter gene polymorphism -1112 C/T is associated with atopic dermatitis in Polish patients

Acta dermatovenerologica Croatica, 2012, Vol.20 (4), p.231-238

2012

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The role of bacterial superantigens in skin diseases

Przegląd dermatologiczny, 2009-07, Vol.96 (4), p.301

2009

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Recurrent Deletion of the Region Encoding Two (Gly-X-Y) Repeats in Patients with Anhidrotic Ectodermal Dysplasia Indicates Important Role for Collagen-Like Domain of the EDA Gene Product—Ectodysplasin-A

Fetal and pediatric pathology, 2000-11, Vol.19 (6), p.425-432

2000

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Recurrent Deletion of the Region Encoding Two (Gly-X-Y) Repeats in Patients with Anhidrotic Ectodermal Dysplasia Indicates Important Role for Collagen-Like Domain of the EDA Gene Product-Ectodysplasin-A

Fetal and pediatric pathology, 2000-01, Vol.19 (6), p.425-432

2000

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Mutations in the EDA gene in three unrelated families reveal no apparent correlation between phenotype and genotype in the patients with an X-linked anhidrotic ectodermal dysplasia

American journal of medical genetics, 2001-05, Vol.100 (3), p.191-197

2001

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Mutations in theEDA gene in three unrelated families reveal no apparent correlation between phenotype and genotype in the patients with an X-linked anhidrotic ectodermal dysplasia

American journal of medical genetics, 2001-05, Vol.100 (3), p.191-197

2001

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Cerebral Palsy in Children as a Risk Factor for Malnutrition

H2O2 and Src-dependent transactivation of the EGF receptor mediates the stimulatory effect of leptin on renal ERK and Na+, K+-ATPase

H 2O 2 and Src-dependent transactivation of the EGF receptor mediates the stimulatory effect of leptin on renal ERK and Na +, K +-ATPase

Indirect CT venography of the abdominal cavity and lower limbs in patients with the suspicion of pulmonary embolism--indications, technique, diagnostic possibilities

Maple Syrup Urine Disease in a newborn infant

Usefulness of telemetric cardiotocography in detection of fetal compromise due to the true knot in umbilical cord

Management of large chronic venous leg ulcers with negative pressure wound therapy

Erythema dyschromicum perstans (ashy dermatosis) – opis przypadków

2-chlorodeoxyadenosine treatment for cutaneous T-cell lymphoma

Erythema dyschromicum perstans (ashy dermatosis) - case reports

Interleukin-13 promoter gene polymorphism -1112 C/T is associated with atopic dermatitis in Polish patients

The role of bacterial superantigens in skin diseases

Recurrent Deletion of the Region Encoding Two (Gly-X-Y) Repeats in Patients with Anhidrotic Ectodermal Dysplasia Indicates Important Role for Collagen-Like Domain of the EDA Gene Product—Ectodysplasin-A

Recurrent Deletion of the Region Encoding Two (Gly-X-Y) Repeats in Patients with Anhidrotic Ectodermal Dysplasia Indicates Important Role for Collagen-Like Domain of the EDA Gene Product-Ectodysplasin-A

Mutations in the EDA gene in three unrelated families reveal no apparent correlation between phenotype and genotype in the patients with an X-linked anhidrotic ectodermal dysplasia

Mutations in theEDA gene in three unrelated families reveal no apparent correlation between phenotype and genotype in the patients with an X-linked anhidrotic ectodermal dysplasia

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