D Branski’s research while affiliated with Hadassah Medical Center and other places

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Publications (132)


Figure 1: Boxes with horizontal lines represent the start of the program; boxes with dots represent at the end of 2 years. The percent BMI is significantly reduced after 2 years of intervention by 5.97%. (*P<0.0001) and when divided by gender, the boys percent BMI is reduced by 5.4% (*P<0.0001) and the girls by 3.6% (#P=0.03); (values±s.e.).
A school-based program of physical activity may prevent obesity
  • Article
  • Full-text available

March 2011

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210 Reads

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14 Citations

European Journal of Clinical Nutrition

Y Shofan

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O Kedar

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D Branski

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[...]

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M Wilschanski

An organized intervention program in pre-pubertal children based on increased physical education and activity together with nutritional advice to the children and their families may prevent obesity. Children aged 9 to 11 received double hours of weekly physical education lessons and additional nutritional advice for 2 years. They were compared with a similar group who received standard physical education lessons only. A total of 82 study and 26 control children completed the 2 years of the project. Boys in the control group gained significantly more weight than the corresponding study group (8.4 kg vs 3.2 kg, respectively (P<0.016)), control delta body mass index (BMI) 1.02 vs study 0.44 (P<0.012). There was no significant change in the weight or BMI in the girls. We conclude that the prevention of obesity may be attained by similar programs. Hormonal effects and compliance at this age may be responsible for the sex differences in this study.

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The Changing Clinical Presentation of Celiac Disease

May 2008

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19 Reads

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28 Citations

Pediatric and Adolescent Medicine

The incidence, the age at presentation and the features of celiac disease (CD) in children have changed considerably over the past 20 years. CD is now believed to be the most common genetically predetermined condition in humans with a prevalence of 1%. Only approximately one third of the patients presents with diarrhea while one third is diagnosed upon screening, and one fifth presents with nonspecific recurrent abdominal pain. Furthermore, it is apparent that most children with CD remain undiagnosed. Another trend is the presentation later in life with atypical symptoms such as anemia, bone disorder and growth failure. The increasing number of CD-associated autoimmune disorders, like insulin-dependent diabetes mellitus, dermatitis herpetiformis, alopecia, Sjögren’s syndrome, autoimmune thyroiditis, autoimmune hepatitis, and atrophic gastritis, is apparent. Currently most patients present with subtle or non-gastrointestinal manifestations at a later age. Median age at presentation of children has shifted from 4 to 8 years.


Nutritional solutions to major public health problems of preschool children: How to optimize growth and development.

January 2006

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1,624 Reads

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1 Citation

Journal of Pediatric Gastroenterology and Nutrition



Urine polymerase chain reaction as a screening tool for detection of congenital cytomegalovirus infection

October 2003

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124 Reads

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55 Citations

Archives of Disease in Childhood - Fetal and Neonatal Edition

To define the incidence of congenital cytomegalovirus (CMV) infection in a defined population in Israel as diagnosed by urine polymerase chain reaction (PCR), and to assess the utility of this method for screening for congenital CMV infection. A convenient sample of urine specimens from asymptomatic newborns were subjected to CMV PCR. Positive results were validated by urine tube culture and by determination of serum CMV IgM antibodies. Maternal CMV IgG was determined in a representative sample of mothers. Newborns with positive urine specimens underwent full clinical evaluation. Epidemiological characteristics of the mothers were extracted from the medical records. Two medical centres in Israel with different population characteristics. A total of 2000 newborns (1000 in each medical centre). Presence of CMV DNA in the urine. Despite significant epidemiological differences between the populations in the two hospitals, the CMV seroprevalence was similar, 80.5% and 85%. Fourteen of the 2000 newborns screened (0.7%) were PCR positive. Urine culture was positive in nine of 10 specimens; IgM was positive in only two of 13 newborns with positive PCR. Eleven newborns underwent full or partial evaluation, and only one (9%) was symptomatic. The incidence of congenital CMV infection in the study population was 0.7%; over 90% were asymptomatic. Urinary CMV PCR is a reliable, rapid, and convenient method, and thus may serve as a screening tool for the detection of congenital CMV infection.


Evaluation of oral budesonide for treatment of mild and moderate exacerbations of Crohn's disease in children

February 2002

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41 Reads

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45 Citations

The Journal of Pediatrics

Oral budesonide has been found to be efficacious for mild to moderate Crohn's disease in adults, with equal improvement rates for budesonide and prednisone. We report the results of a retrospective study of budesonide treatment in mild to moderate Crohn's disease in children. Charts of patients treated with budesonide (n = 62) with a pediatric Crohn's Disease Activity Index of 12.5 to 40 were compared with a cohort of 58 age-matched patients treated with prednisone. Among children treated with budesonide, 48% had remission compared with 77% of the children treated with prednisone (P =.001). Among patients who had failed previous medical therapy with mesalamine, 59% had remission with budesonide (9 mg/day). Remission with prednisone occurred in 73% of children who failed to achieve remission with budesonide. Patients responding to budesonide had significantly milder disease compared with nonresponders who had remission while taking prednisone. Budesonide is useful in mild to moderate Crohn's disease in children. It is more effective than mesalamine and antibiotics but less effective than prednisone. Budesonide should be considered for first-line therapy in mild to moderate Crohn's disease.


Ethnic differences in cigarette smoking among adolescents: A comparison of Jews and Arabs in Jerusalem

July 2001

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19 Reads

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12 Citations

The Israel Medical Association journal

Prevention of cigarette smoking is an important issue in public health policy. Since most adult smokers began smoking in childhood, understanding behavorial factors associated with smoking initiation would contribute to smoking initiation programs. Health-related behavior may vary between different ethnic groups. To determine the prevalence of smoking among Jewish and Arab adolescents in Jerusalem, and whether there are differences in smoking initiation between the two ethnic groups. We carried out a cross-sectional survey of all students in the 6th to 11th grades (age range 11-17 years) of a Jewish school and an Arab school in the Jerusalem area, using an anonymous self-completion questionnaire. A total of 791 questionnaires was analyzed, 479 from the Jewish students and 312 from the Arab students. The lowest prevalence of smoking was found among Arab female students and the highest among Jewish female students (9% vs. 41%, P < 0.001). The prevalence of smoking among Jewish and Arab males was similar. More Arab female students smoked than their mothers. Peer pressure seemed to be a more important factor among Jewish students. This study demonstrated the presence of ethnic differences in smoking prevalence and the reasons for smoking among adolescents in Israel. These results suggest the need for specific smoking prevention policies for different ethnic groups.



Leukocyte adhesiveness/aggregation test (LAAT) to discriminate between viral and bacterial infections in children

June 2000

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37 Reads

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20 Citations

Acta Paediatrica

We previously noted that white blood cells (WBC) have increased adhesive properties during bacterial infections. Here, we aim to explore the possibility of using the different adhesive properties of WBC as a means of differentiating between viral and bacterial infections, a common problem in paediatrics. The adhesive properties of WBC in the peripheral blood of 25 children with documented bacterial infections, 15 with documented viral infections and 36 with probable viral infections, were studied by means of a leukocyte adhesiveness/aggregation slide test (LAAT). The results of the LAAT were compared with those of the other acute phase reactants, namely WBC, differential count and erythrocyte sedimentation rate (ESR), which were taken in the same blood sample in each patient. The sensitivity, specificity and positive predictive value were 92%, 96%, and 92%, respectively for the LAAT; 83%, 87% and 80% for the ESR; 56%, 78% and 56% for the white blood cell count; and 54%, 74% and 50% for the differential count. The presence of bacterial infections in children can be tested using a simple slide test to reveal the increased state of leukocyte adhesiveness/aggregation in the peripheral blood. The LAAT is a reliable, rapid and inexpensive test, and it can be a useful laboratory tool for the paediatrician treating a child with acute febrile illness.


Citations (61)


... The scientific and medical literature is rich in comprehensive reviews describing EIM in CD populations. As can be expected, the list is expanding rapidly since the 90th [38] to the present [39][40][41]. Fig. 1 describes the multiple faces of the disease. ...

Reference:

Autoimmunity in celiac disease: Extra-intestinal manifestations
Extra intestinal manifestation and associated disorders of celiac disease
  • Citing Article
  • January 1992

... In the past, children were diagnosed with CD at the approximate age of 4 years old, however during the recent years it has been observed a trend in diagnosing children later, at the age of 8 years old. This is due to the evolving pattern of clinical presentation of this disease, with more and more cases presenting with atypical and vague symptoms [14]. Clinical representation varies depending on an age group of the patients, with younger children more likely to experience gastrointestinal symptoms, and the older presenting extraintestinal signs. ...

The Changing Clinical Presentation of Celiac Disease
  • Citing Article
  • May 2008

Pediatric and Adolescent Medicine

... Residual function variants are characterized by pancreatic sufficiency, lower mortality, and milder pulmonary disease, although a substantial proportion have significant life-shortening pulmonary disease [3]. The CFTR gene was discovered in 1989, enabling the identification of disease-causing variants, first in affected families and later in the general population [4]. In 2001, upon joint recommendation by the American College of Medical Genetics and Genomics and the American College of Obstetricians and Gynecologists, CF became the first target of pan-ethnic universal population genetic carrier screening (PGCS) [5]. ...

Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in Israel
  • Citing Article
  • August 1995

Human Genetics

... The rest were studies with some concerns [28,34,37,39,48] or low risk of bias [29,33,36]. For the quasiexperiments, seven out of nine studies were rated as serious risk of bias [35,40,[46][47][48]50,51] that was mostly due to insufficient control of possible bias from either possible confounders or dropouts, and/or selective reporting of findings. Other studies were rated as moderate risk of bias [38] or low risk of bias [26]. ...

A school-based program of physical activity may prevent obesity

European Journal of Clinical Nutrition

... In CD intestinal villi are flattened and shortened , the epithelial cells damaged and increased the depth of crypt layer this all will compromise the intestinal absorption ( Murray JA , 1999) Patients with CD have a high requirement for repairing the intestinal tissue and there is an increase of the conversion of EFA into eicosanoids , so this together with compromised intestinal absorption will lead to the patient with CD is predicted to be at a high risk for having essential fatty acid deficiency ( Branski D, et al 1992) Patients with active CD had increased Palmitoleic ( 16:1n-7 ) , Oleic (18:1n-9) and Mead acid (20:3n-9) (Steel , Daniella M. , et al 2006) ...

Eicosanoids Content in Small Intestinal Mucosa of Children with Celiac Disease
  • Citing Article
  • March 1992

Journal of Pediatric Gastroenterology and Nutrition

... As one of the few documented cases of purpura fulminans resulting from invasive Hi infection originating from epiglottitis in the adult population, it is essential to emphasize the severity of such infections in a post-vaccination era, especially in adult patients, in which the clinical presentation may deviate from the conventional patterns observed in the pediatric population [6,7]. The epidemiological landscape of invasive Hi disease has undergone notable changes after the widespread vaccination implementation, as Hib previously accounted for over 90% of Hi-invasive diseases, with a remarkable reduction in both infection and colonization [2]. ...

Haemophilus influenzae type b purpura fulminans treated with hyperbaric oxygen
  • Citing Article
  • October 1992

Journal of Infection

... The etiology of BE is associated with different conditions such as esophageal atresia with or without trachea-esophageal fistulas (EA/TEF), congenital diaphragmatic hernias, hiatus hernias, mental retardation, cerebral palsy, Cornelia De Lange Syndrome and Raynaud's phenomenon [1,[9][10][11][12][13]. The lag time to developing metaplasia from the time of initial surgical correction is about 10 years [12,14]. ...

Barrett's esophagus in a young patient with Raynaud's phenomenon
  • Citing Article
  • December 1991

The Journal of Rheumatology

... All DLD patients with DBS hypercitrullinemia (n = 3) have been symptomatic at the time of collection, suggesting that citrulline elevations may only occur during times of metabolic decompensation [15]. Indeed, all previously reported DLD patients with plasma hypercitrullinemia, including both Patients 1 and 2 (data not shown), have only displayed plasma citrulline elevations during metabolic decompensations, with normalization when clinically well [5,18,19]. Although the mechanism for the accumulation of citrulline in DLD deficiency is unknown, Haviv et al. propose that it may be a result of insufficient oxaloacetate production, with secondary aspartate depletion and subsequent interference with argininosuccinate formation in the urea cycle [15]. ...

Recurrent, familial Reye-like syndrome with a new complex amino and organic aciduria
  • Citing Article
  • August 1990

European Journal of Pediatrics

... Recognizing these conditions is crucial as they present unique diagnostic challenges as all the indirect tests are based on a single enzyme secretion, e.g. the generally used FE-1 based on elastase assessment, therefore misses isolated, amylase, lipase and trypsin deficiencies. Lipase Deficiency results in fat malabsorption, leading to steatorrhea, weight loss, and fat-soluble vitamin deficiencies [35,36]. ...

Isolated lipase and colipase deficiency in two brothers
  • Citing Article
  • January 1991

Gut

... HAV, the causal agent of hepatitis A, is transmitted fecal-orally, typically presents with acute gastrointestinal manifestations, and rarely causes death 62 . This patient's symptoms are not consistent with the textbook presentation of hepatitis A, though cases of neurological sequelae associated with HAV have been documented [63][64][65][66] . We thus interpret the metagenomic sequencing results with caution, as it is possible that HAV is an incidental finding. ...

Seizures in the course of hepatitis A
  • Citing Article
  • March 1990

American Journal of Diseases of Children (1960)