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Acute cardiac effects of carbon monoxide poisoning in children

European journal of emergency medicine, 2010-08, Vol.17 (4), p.192-196

2010

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The analysis of child abuse and neglect cases assessed by a multidisciplinary study group between 2005-2008

Turkish journal of pediatrics, 2012-07, Vol.54 (4), p.333-343

2012

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Answer

Pediatric nephrology (Berlin, West), 2003-09, Vol.18 (9), p.964-965

2003

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Answer

Pediatric nephrology (Berlin, West), 2003-09, Vol.18 (9), p.964

2003

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Apoptosis and proliferation in childhood acute proliferative glomerulonephritis

Pediatric nephrology (Berlin, West), 2005-11, Vol.20 (11), p.1572-1577

2005

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Assessment of left ventricular systolic and diastolic functions in children with merosin-positive congenital muscular dystrophy

International journal of cardiology, 2003-02, Vol.87 (2), p.129-133

2003

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Autoimmune hemolytic anemia and giant cell hepatitis: Report of three infants

Turkish journal of haematology, 2010-12, Vol.27 (4), p.308-313

2010

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Autoimmune hemolytic anemia and giant cell hepatitis: Report of three infants

Turkish journal of haematology, 2010-12, Vol.27 (4), p.308-313

2010

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Autoimmune hemolytic anemia and giant cell hepatitis: report of three infants / Otoimmun hemolitik anemi ve dev hucreli hepatit birlikteligi olan uc olgunun sunumu

Turkish journal of haematology, 2010-12, Vol.27 (4), p.308

2010

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An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker–Warburg syndrome (WWS) caused by a mutation in the POMT1 gene

Neuromuscular disorders : NMD, 2005-04, Vol.15 (4), p.271-275

2005

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Bilateral adrenal cystic neuroblastoma with hepatic and splenic involvement in a newborn

Journal of pediatric hematology/oncology, 2005-12, Vol.27 (12), p.670-671

2005

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Burnout syndrome during residency in internal medicine and pediatrics in a country without working time directive

International journal of health care quality assurance, 2014-01, Vol.27 (3), p.223-230

2014

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Cardiac lymphangioma

The American heart journal, 1991-06, Vol.121 (6), p.1821-1824

1991

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Childhood intrathoracic Hodgkin lymphoma with hypertrophic pulmonary osteoarthropathy: a case report and review of the literature

European journal of pediatrics, 2008-04, Vol.167 (4), p.419-423

2008

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Cirrhosis in children with celiac disease

Journal of clinical gastroenterology, 2005-08, Vol.39 (7), p.630-633

2005

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Classification of congenital muscular dystrophy

The Journal of pediatrics, 1990-07, Vol.117 (1), p.166-166

1990

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Clinical and histopathological study of merosin-deficient and merosin-positive congenital muscular dystrophy

Pediatric and developmental pathology, 2000-03, Vol.3 (2), p.168-176

2000

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Clinical features and treatment results in children with anaplastic large cell lymphoma

Turkish journal of pediatrics, 2015-09, Vol.57 (5), p.458-466

2015

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Clinical Features and Treatment Results of Children with Diffuse Large B-Cell Lymphoma

Pediatric hematology and oncology, 2014-09, Vol.31 (6), p.509-517

2014

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Clinical quiz. Questions and answer

Pediatric nephrology (Berlin, West), 2003, Vol.18 (9), p.962-965

2003

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Clinicopathological and immunohistological features in childhood IgA nephropathy: a single-centre experience

Clinical kidney journal, 2013-04, Vol.6 (2), p.169-175

2013

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Common deletion of mitochondrial DNA in a 5-year-old girl with failure to thrive, ptosis, ophthalmoplegia and ragged-red fibers

Brain & development (Tokyo. 1979), 1999-09, Vol.21 (6), p.413-415

1999

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A comparative histopathologic evaluation of the effects of three different solutions used for whole bowel irrigation: An experimental study

Journal of pediatric surgery, 2000-04, Vol.35 (4), p.564-568

2000

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Congenital muscular dystrophy (non-fukuyama type) in Turkey: A clinical and pathological evaluation

Brain & development (Tokyo. 1979), 1989, Vol.11 (5), p.341-344

1989

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A Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities Caused by Defective De Novo Phosphatidylcholine Biosynthesis

American journal of human genetics, 2011-06, Vol.88 (6), p.845-851

2011

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Acute cardiac effects of carbon monoxide poisoning in children

The analysis of child abuse and neglect cases assessed by a multidisciplinary study group between 2005-2008

Answer

Answer

Apoptosis and proliferation in childhood acute proliferative glomerulonephritis

Assessment of left ventricular systolic and diastolic functions in children with merosin-positive congenital muscular dystrophy

Autoimmune hemolytic anemia and giant cell hepatitis: Report of three infants

Autoimmune hemolytic anemia and giant cell hepatitis: Report of three infants

Autoimmune hemolytic anemia and giant cell hepatitis: report of three infants / Otoimmun hemolitik anemi ve dev hucreli hepatit birlikteligi olan uc olgunun sunumu

An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker–Warburg syndrome (WWS) caused by a mutation in the POMT1 gene

Bilateral adrenal cystic neuroblastoma with hepatic and splenic involvement in a newborn

Burnout syndrome during residency in internal medicine and pediatrics in a country without working time directive

Cardiac lymphangioma

Childhood intrathoracic Hodgkin lymphoma with hypertrophic pulmonary osteoarthropathy: a case report and review of the literature

Cirrhosis in children with celiac disease

Classification of congenital muscular dystrophy

Clinical and histopathological study of merosin-deficient and merosin-positive congenital muscular dystrophy

Clinical features and treatment results in children with anaplastic large cell lymphoma

Clinical Features and Treatment Results of Children with Diffuse Large B-Cell Lymphoma

Clinical quiz. Questions and answer

Clinicopathological and immunohistological features in childhood IgA nephropathy: a single-centre experience

Common deletion of mitochondrial DNA in a 5-year-old girl with failure to thrive, ptosis, ophthalmoplegia and ragged-red fibers

A comparative histopathologic evaluation of the effects of three different solutions used for whole bowel irrigation: An experimental study

Congenital muscular dystrophy (non-fukuyama type) in Turkey: A clinical and pathological evaluation

A Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities Caused by Defective De Novo Phosphatidylcholine Biosynthesis

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