# عنوان نوع فایل سایز فایل بازدید دانلود امتیاز قیمت (تومان)
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Urticaria due to Urtica dioica in a neonate
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Pediatric oncology for the general pediatrician
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Acquired nonscarring diffuse hair loss in a 3-year-old girl
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A novel WT1 gene mutation in a patient with Wilms’ tumor and 46, XY gonadal dysgenesis
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A case report of hyperthyroid-associated thymic hypertrophy in a child, presenting as an anterior mediastinal mass
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N-carbamylglutamate treatment for acute neonatal hyperammonemia in isovaleric acidemia
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Early congenital syphilis in a premature baby
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Ovarian cyst torsion in a patient with congenital lipoid adrenal hyperplasia
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Household poisoning cases from mercury brought from school
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Dyggve–Melchior–Clausen syndrome: novel splice mutation with atlanto-axial subluxation
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Combination therapy for life-threatening pulmonary hypertension in a premature infant: first report on bosentan use
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Relevant factors influencing flatfoot in preschool-aged children
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Doppler manifestations of ductal steal: role in decision making
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Destructive pulmonary staphylococcal infection in a boy with hyper-IgE syndrome: a novel mutation in the signal transducer and activator of transcription 3 (STAT3) gene (p.Y657S)
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Congenital acute lymphoblastic leukemia: a two-case report and a review of the literature
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Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy
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Nephrotic syndrome occurring during tiopronin treatment for cystinuria
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Use of milrinone in the management of haemodynamic instability following duct ligation
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LEOPARD syndrome (PTPN11, T468M) in three boys fulfilling neurofibromatosis type 1 clinical criteria
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Attention-deficit hyperactivity disorder in children chronically exposed to high level of vehicular pollution
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Cerebral hemiatrophy associated with hippocampal sclerosis following a single prolonged febrile seizure
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Fatal group A Streptococcus purpura fulminans in a child receiving TNF-ل blocker
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de Quervain thyroiditis in a young boy following hand–foot–mouth disease
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Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations
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Chronic pancreatitis in branched-chain organic acidurias—a case of methylmalonic aciduria and an overview of the literature
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Urticaria due to Urtica dioica in a neonate

Urticaria due to Urtica dioica ...

Urticaria is one of the most common dermatoses during the childhood, but it is very rare in the neonates. A 17-day-old infant with a generalized urt ...

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Pediatric oncology for the general pediatrician

Pediatric oncology for the gene ...

Since its establishment as a pediatric subspecialty oncology has become the near exclusive domain of specialized tertiary centers. This has greatly ...

77.08 KB
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Acquired nonscarring diffuse hair loss in a 3-year-old girl

Acquired nonscarring diffuse ha ...

A 3-year-old girl showed fine, sparse, and brittle scalp hair without signs of cicatricial cutaneous alterations. Dermoscopy as well as scanning ele ...

92.92 KB
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A novel WT1 gene mutation in a patient with Wilms’ tumor  and 46, XY gonadal dysgenesis

A novel WT1 gene mutation in a ...

Denys–Drash syndrome (DDS) is a rare genetic disorder featuring the triad ofWilms' tumor, early-onset renal failure, and 46, XY disorder of sex deve ...

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A case report of hyperthyroid-associated thymic  hypertrophy in a child, presenting as an anterior  mediastinal mass

A case report of hyperthyroid-a ...

We present the case of an 8-year-old boy with an anterior mediastinal mass and signs of hyperthyroidism. The anterior mediastinal mass had radiologi ...

125.19 KB
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N-carbamylglutamate treatment for acute neonatal  hyperammonemia in isovaleric acidemia

N-carbamylglutamate treatment f ...

Hyperammonemia occurs mainly in patients with branched-chain organic acidemias such as propionic, methylmalonic, and isovaleric acidemias. Its patho ...

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Early congenital syphilis in a premature baby

Early congenital syphilis in a ...

In the UK, diagnosis of syphilis among women of child-bearing age has more than doubled between 1999 and 2007, and each year, around ten cases of co ...

89.69 KB
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Ovarian cyst torsion in a patient with congenital lipoid  adrenal hyperplasia

Ovarian cyst torsion in a patie ...

Congenital lipoid adrenal hyperplasia (CLAH) is the most severe form of congenital adrenal hyperplasia, characterized by lack of synthesis of all go ...

175.77 KB
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Household poisoning cases from mercury brought  from school

Household poisoning cases from ...

Mercury has a number of unique and fascinating properties. It is present in the environment in several forms, both organic and inorganic. Each of th ...

دانلود 1
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Dyggve–Melchior–Clausen syndrome: novel splice mutation  with atlanto-axial subluxation

Dyggve–Melchior–Clausen syndrom ...

Dyggve–Melchior–Clausen (DMC) syndrome is a rare autosomal recessive disorder characterized by the association of a progressive spondyloepimetaphyse ...

دانلود 1
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Combination therapy for life-threatening pulmonary  hypertension in a premature infant: first report  on bosentan use

Combination therapy for life-th ...

Premature infants with preterm premature rupture of membranes (PPROM) are at high risk of severe respiratory failure because of lung hypodysplasia a ...

105.17 KB
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Relevant factors influencing flatfoot  in preschool-aged children

Relevant factors influencing fl ...

The aim of this study was to discuss the influence of age, gender, obesity status, joint laxity, and the W-sitting habit on flatfoot in preschool-ag ...

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Doppler manifestations of ductal steal:  role in decision making

Doppler manifestations of ducta ...

Patent ductus arteriosus in extremely premature babies is associated with major neonatal morbidities such as necrotizing enterocolitis and intravent ...

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Destructive pulmonary staphylococcal infection in a boy  with hyper-IgE syndrome: a novel mutation  in the signal transducer and activator  of transcription 3 (STAT3) gene (p.Y657S)

Destructive pulmonary staphyloc ...

Hyper IgE syndrome (HIES) is a rare primary immunodeficiency disorder, characterized by eczema, recurrent skin and lung infections, and significantl ...

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Congenital acute lymphoblastic leukemia: a two-case report  and a review of the literature

Congenital acute lymphoblastic ...

Congenital leukemia is a rare disease with particular biological and clinical characteristics which differs from those of older children and adults. ...

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Two siblings with triple A syndrome and novel mutation  presenting as hereditary polyneuropathy

Two siblings with triple A synd ...

The clinical and molecular data on triple A syndrome in two siblings (girl 3.5 years and boy 5.5 years at presentation) with early onset of neurolog ...

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Nephrotic syndrome occurring during tiopronin treatment  for cystinuria

Nephrotic syndrome occurring du ...

Cystinuria is an autosomal recessive disorder characterized with abnormal tubular reabsorption of cystine and dibasic amino acids leading to cystine ...

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Use of milrinone in the management of haemodynamic  instability following duct ligation

Use of milrinone in the managem ...

Haemodynamic instability affects 22% to 29% of very low birth weight infants in the acute period following ligation of the ductus arteriosus and con ...

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LEOPARD syndrome (PTPN11, T468M) in three boys  fulfilling neurofibromatosis type 1 clinical criteria

LEOPARD syndrome (PTPN11, T468M ...

Noonan syndrome (NS) and neurofibromatosis type 1 (NF1) are well-defined entities. The association of both disorders is called neurofibromatosis–Noo ...

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Attention-deficit hyperactivity disorder in children  chronically exposed to high level of vehicular pollution

Attention-deficit hyperactivity ...

The purpose of this study is to explore whether sustained exposure to vehicular air pollution affects the behavior and activities of children. The p ...

دانلود 1
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Cerebral hemiatrophy associated with hippocampal sclerosis  following a single prolonged febrile seizure

Cerebral hemiatrophy associated ...

The etiological relation of prolonged febrile seizures with hippocampal sclerosis and cerebral hemiatrophy is controversial. Causal relationship is ...

575.48 KB
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Fatal group A Streptococcus purpura fulminans in a child  receiving TNF-ل blocker

Fatal group A Streptococcus pur ...

Inhibition of tumor necrosis factor alpha (TNF-ل) is effective in the treatment of many pediatric autoimmune diseases and inflammatory conditions. C ...

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de Quervain thyroiditis in a young boy following  hand–foot–mouth disease

de Quervain thyroiditis in a yo ...

de Quervain thyroiditis, also known as subacute thyroiditis, is a self-limited inflammatory disease of the thyroid gland. It is extremely rare in ch ...

121.17 KB
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Effect of cyclosporin A on proteinuria in the course  of glomerulopathy associated with WT1 mutations

Effect of cyclosporin A on prot ...

Denys–Drash syndrome (DDS) is characterized by progressive glomerulopathy caused by diffuse mesangial sclerosis (DMS), genitourinary defects, and a ...

84.44 KB
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Chronic pancreatitis in branched-chain organic  acidurias—a case of methylmalonic aciduria  and an overview of the literature

Chronic pancreatitis in branche ...

A severe rare complication in patients with branched-chain organic acidurias (BCOA) is pancreatitis with a limited number of patients published so f ...

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