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800 Etiology and Outcome of Hydrops Fetalis: A Single Center Experience in Turkey

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A229-A230

2012

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Xanthoma disseminatum: A child with respiratory system involvement and bronchiectasis

Pediatric pulmonology, 2005-01, Vol.39 (1), p.84-87

2005

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A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey

Annals of neurology, 1997-08, Vol.42 (2), p.222-229

1997

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A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families

Journal of medical genetics, 2000-05, Vol.37 (5), p.361-367

2000

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Transverse testicular ectopia with persistent müllerian duct syndrome

Journal of pediatric surgery, 1997-09, Vol.32 (9), p.1362-1364

1997

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Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature

Neuropediatrics, 2002-12, Vol.33 (6), p.314-319

2002

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Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R

Haematologica (Roma), 2015-06, Vol.100 (6), p.e216-e219

2015

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G.P.17.03 Muscle histopathology in asymptomatic children with incidentally detected high CK

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.655-655

2009

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Primary lacrimal sac non-Hodgkin's lymphoma in a child

International journal of pediatric otorhinolaryngology, 2005-11, Vol.69 (11), p.1551-1553

2005

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Leigh Syndrome in a 3-Year-Old Boy with Unusual Brain MR Imaging and Pathologic Findings

American journal of neuroradiology : AJNR, 2000-01, Vol.21 (1), p.224-227

2000

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G.P.2.01 Frequency of different forms of congenital muscular dystrophies in a referral center

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.735-735

2008

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G.P.3.01 Clinical and histopathological features in muscle biopsies of children with suspected mitochondrial disease

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.751-752

2008

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Ectopic Thymic Tissue as a Rare and Confusing Entity

European journal of pediatric surgery, 2002-10, Vol.12 (5), p.327-329

2002

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Undifferentiated (embryonal) sarcoma of the liver: an intriguing diagnosis in a child

European journal of pediatric surgery, 2009-10, Vol.19 (5), p.328-330

2009

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Al‐Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2‐Related Disorders

Journal of bone and mineral research, 2023-05, Vol.38 (5), p.692-706

2023

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Inflammatory pseudotumor causing intestinal obstruction: Diagnostic and therapeutic aspects

Journal of pediatric surgery, 1998-12, Vol.33 (12), p.1843-1845

1998

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Lymphoproliferative disorders in patients with primary immuno-deficiencies

Paediatric respiratory reviews, 2011, Vol.12, p.S79-S80

2011

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Polyarteritis Nodosa Involving the Hepatobiliary System in an Eight-Year-Old Girl with a Previous Diagnosis of Familial Mediterranean Fever

European journal of pediatric surgery, 2000-04, Vol.10 (2), p.145-147

2000

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Endobronchial Leiomyoma in Children

European journal of pediatric surgery, 2000-04, Vol.10 (2), p.136-139

2000

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C.P.2.12 Congenital muscular dystrophy with mental retardation, dilated cardiomyopathy and abnormally located mitochondria

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.847-847

2007

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C.P.3.07 Muscle pathology in alpha-dystroglycanopathies with central nervous system malformation

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.871-872

2007

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A homozygous nonsense mutation in δ-sarcoglycan exon 3 in a case of LGMD2F

Neuromuscular disorders : NMD, 2000-06, Vol.10 (4), p.247-250

2000

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Pulmonary involvement in a child with ligneous conjunctivitis and homozygous type I plasminogen deficiency

Pediatric pulmonology, 2001-08, Vol.32 (2), p.179-183

2001

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Diagnostic difficulties in neuronal intestinal dysplasia and segmental colitis

Journal of pediatric surgery, 2000-03, Vol.35 (3), p.519-521

2000

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PO-0271 A Difficult Diagnosis Of Natural Killer Cell Lymphoma Presenting With Bilateral Pleural Effusions

Archives of disease in childhood, 2014-10, Vol.99 (Suppl 2), p.A333-A334

2014

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800 Etiology and Outcome of Hydrops Fetalis: A Single Center Experience in Turkey

Xanthoma disseminatum: A child with respiratory system involvement and bronchiectasis

A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey

A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families

Transverse testicular ectopia with persistent müllerian duct syndrome

Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature

Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R

G.P.17.03 Muscle histopathology in asymptomatic children with incidentally detected high CK

Primary lacrimal sac non-Hodgkin's lymphoma in a child

Leigh Syndrome in a 3-Year-Old Boy with Unusual Brain MR Imaging and Pathologic Findings

G.P.2.01 Frequency of different forms of congenital muscular dystrophies in a referral center

G.P.3.01 Clinical and histopathological features in muscle biopsies of children with suspected mitochondrial disease

Ectopic Thymic Tissue as a Rare and Confusing Entity

Undifferentiated (embryonal) sarcoma of the liver: an intriguing diagnosis in a child

Al‐Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2‐Related Disorders

Inflammatory pseudotumor causing intestinal obstruction: Diagnostic and therapeutic aspects

Lymphoproliferative disorders in patients with primary immuno-deficiencies

Polyarteritis Nodosa Involving the Hepatobiliary System in an Eight-Year-Old Girl with a Previous Diagnosis of Familial Mediterranean Fever

Endobronchial Leiomyoma in Children

C.P.2.12 Congenital muscular dystrophy with mental retardation, dilated cardiomyopathy and abnormally located mitochondria

C.P.3.07 Muscle pathology in alpha-dystroglycanopathies with central nervous system malformation

A homozygous nonsense mutation in δ-sarcoglycan exon 3 in a case of LGMD2F

Pulmonary involvement in a child with ligneous conjunctivitis and homozygous type I plasminogen deficiency

Diagnostic difficulties in neuronal intestinal dysplasia and segmental colitis

PO-0271 A Difficult Diagnosis Of Natural Killer Cell Lymphoma Presenting With Bilateral Pleural Effusions

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