Publications

  1. Acute leukemia in the North East Egypt: Survival studies. Annual Meeting for European Society of pediatric hematology, Turkey, 1998.
  2. Undescended testes: Early forecasting cases candidates for surgery. Published in Egyptian Journal of Surgery, 1998. Presented as booster in the ESPR (European Society of Pediatric research), Copenhagen, 1999.
  3. A 15-years experience in Neuroblastoma: Survival studies. Annual Conference of European Society of Pediatric oncology, Japan, 1999.
  4. Renal hemodynamic changes in children with liver cirrhosis. Journal of Pediatric Nephrology, 1999 Nov; 13(9):854-8.
  5. M. Hafez, Z. El-Morsy, A. Settin, Mohammad Al-Haggar, R. Al-Baz, Y. Al-Tonbary, N. Abdelrazik, T. El-Desoky, A. Shaltout, A. Mansour, H. El-Marsafaway: Gene mutations in Glucose-6-Phosphate Dehydrogenase in Egypt. (Published in the Egyptian Journal of Pediatrics, 2001, Accepted as oral presentation in 7th Annual Meeting of the European Hematology Association – Florence, Italy, 6-9 June 2002. Supplement in The Hematology Journal, Abst. No. 0631).
  6. Growth parameters and obesity in Egyptian children (Egyptian Journal of Epidemiology and Public health, 2002).
  7. New trends in treatment of Bronchial asthma: UPDATES; Asthma Club held at Le Gulf Meredian, Saudi Arabia, on February, 2002, Sponsored by MSD company.
  8.  How to make a successful medical presentation? Free talk done for specialists and consultants in Eastern province KSA at May, 2003, in Al-Kosaibi Hotel sponsored by Schering USA.
  9. Frequency of AZF gene microdeletions among Infertile Men with Idiopathic Oligozoospermia and Azoospermia in Nile Delta regions of Egypt. [Egyptian Journal of Dermatology and Andrology 2004; Volume 24, No (1, 2, 3, 4):65-78].
  10.  Mohammad Al-Haggar, Hala Al-Marsafawy, Nabeel Abdel-Razek, Rizk Al-Baz, Abdel-Hamid Mostafa: Acute painful crises of sickle cell disease in Egyptian children: predictors of severity for preventive strategy. (The International Journal of Hematology, Japanese Society of Hematology; Int J Hematol 2006; 83(3): 224-228).
  11.  Ahmad Settin, Mohammad Al-Haggar, Hala El-Marsafawy, Amal Abd-Alkader, Rizk Al-Baz, Ahmad Mansour, Rabab Ali, Eman Alam: Genetic analysis of rheumatic fever among Egyptian families: Consanguinity pattern, Segregation analysis and Blood group association. (Journal of Medical Sciences – Pakistan);  J Med Sci 2006 May – June 6(3): 415-422.
  12.  Recurrent otitis media in children: Relation to serum immunoglobulin G level. (The Medical Journal of Cairo University June 2004; Volume 72, No. 2 Supp; 55-60).
  13.  Long-term oral iron supplementation in breast-fed infants: Impact on growth parameters and general health. (Benha Medical Journal; Volume 21, No. 2 May, 2004).
  14.  Hepato-pulmonary syndrome in children with cirrhosis: Echocardiographic findings (Benha Medical Journal, Volume 21, No. 2 May, 2004).
  15.  Mohammad Al-Haggar, Mohamed Ragab, Manal Awad, Rizk Al-Baz: Soluble adhesion molecules in juvenile idiopathic arthritis: Relation to activity and clinical subtype. (Accepted oral presentation in the 29th UMEMPS Congress (Union of Middle East and Mediterranean Pediatric Societies) 14th -17th September, 2005; Abst Ref (55). Journal of Medical Sciences – Pakistan; J Med Sci 2006 May – June 6(3): 492-497.  
  16.  Mohammad Al-Haggar, Mohamed Ragab, Manal Awad, Rizk Al-Baz: Soluble adhesion molecules in rheumatic fever: Relation to pathogenesis and disease activity; Extracted from Master degree Thesis: Study of some adhesion molecules in children with rheumatic fever; Accepted oral presentation in the 29th UMEMPS Congress (Union of Middle East and Mediterranean Pediatric Societies) 14th –17th September, 2005; Abst Ref (52).
  17.  Mohammad Al-Haggar, Ahmad Settin, Mona Gouida, Rizk Al-Baz, Rabab Abu Alkasem, Seham Al-Mansi, Tarek Attia, Zakaria Al-Morsy: Case Report: Early diagnosis of Hodgkin’s disease based on Flow Cytometry parameters (Accepted in British Medical Journal-Middle East at July, 2005; Published in September, 2005; Vol. 12 No. 129:14-15).
  18.  Mohammad Al-Haggar, Zienab Al-Naggar, Mohammad Abdel-Salam: Biofeedback and cognitive behavioral therapy for Egyptian adolescents suffering from chronic fatigue syndrome. (Accepted oral presentation in the International Pediatric congress of King Fahd Military Complex at 2004 -Accepted oral presentation in the 29th UMEMPS Congress (Union of Middle East and Mediterranean Pediatric Societies) 14th –17th September, 2005; Abst Ref (54). Journal of Pediatric Neurology, www.jpneurology.org; J Ped Neurol 4(3): 161-169.
  19.  Ahmad Settin, Mohammad Al-Haggar, Rizk Al-Baz, Mostafa Al-Aiouty, Mohammad Hafez: Screening of mentally handicapped Egyptian children for Fragile X Syndrome using clinical, cytogenetic and molecular Approaches. Journal of Pediatric Neurology, www.jpneurology.org; J Ped Neurol 3(4): 217-225.
  20.  Mohammad Al-Haggar, Rizk El-Baz, Hisham Youseff, Nierra Othman, Rabab Ali: Overview on attention deficit hyperactivity disorder among children from Delta regions of Egypt (A 10 years-study). Journal of Pediatric Neurology, www.jpneurology.org; J Ped Neurol 4(1): 15-18.
  21.  Mohammad Al-Haggar, Mostafa Al-Aiouty, Mohammad Ragab, Soheir Yehia: Neurophysiologic Evaluation of Peripheral Nerve Function in Uremic Egyptian Children. Journal of Pediatric Neurology, www.jpneurology.org; J Ped Neurol 4(2): 89-95.
  22.  Ahmad Settin, Mohammad Al-Haggar, Rizk Al-Baz, Hisham Yousof, Nayera Osman: Screening for G6PD Mediterranean mutation among Egyptian neonates with high or prolonged jaundice. Hema Journal; the Journal of Hellenic Society of Hematology; Haema 2006; 9(1): 83-90.
  23.  Ahmad Settin, Mohammad Al-Haggar, Mona Gouida, Rizk Al-Baz, Rabab Abu Alkasem, Seham Al-Mansi, Tarek Attia, Zakaria Al-Morsy: Diagnostic  Significance  of  Flow  Cytometric  Analysis  of  DNA Ploidy and Apoptosis in Children with  Lymphadenopathy. Hema Journal; the Journal of Hellenic Society of Hematology; Haema 2006; 9(2): 240-246.
  24.  Ahmad Settin, Mohammad Al-Haggar, Mostafa Neamatallah, Afaf Al- Said, Mohammad Hafez: Detection of Beta-thalassemia Mutations Using Primer-Specific Amplification Compared to Reversed Dot Blot Hybridization Technique in Egyptian Cases. Hema Journal; the Journal of Hellenic Society of Hematology; Haema 2006; 9(3): 401-409.
  25.  Mohammad Al-Haggar, Nermin Yahia, Hussam Ghanem: High dairy calcium intake in pubertal girls: Relation to body weight gain and bone mineral status. (Journal of Medical Sciences – Pakistan);  J Med Sci 2006 (July- August); 6(4):631-635.
  26.  Mohammad Al-Haggar, Ahmad Settin, Mohammad Ragab, May Al-Shahat, Hisham Abdel-Hadi, El-Shahat Toson, Mona Samy, Rabab Abo-El-Kasem, Soheir Yahia, Zakaria Al-Morsi: Segregation analysis of P53, c-myc, DNA ploidy using flow cytometry among Egyptian families with childhood leukemia. Journal of Medical Science; Pakistan. J Med Sci 2006 (November – December); 6(6): 906-914.
  27.  Ahmad Settin, Tarek Al-Dosokey, Mohammad Al-Haggar, Mahmoud Al-Bendary, Mohammad Ezz, Rizk Al-Baz, Amr El-Shahed, Rabab Abo Al-Kasem: Increased risk of liver cirrhosis among Egyptian carriers of S and/or Z mutant alleles of Alpha1 anti-trypsin gene. Arab J Gastroenterol 2006; 7(1): 14-18.
  28. Ahmad Settin, Tarek Al-Dosokey, Mohammad Al-Haggar, Mahmoud El-Bendary, Mohammad Ezz, Rizk El Baz, Amr El-Shahed, Rabab Abo-Al-Kassem. C282Y and H63D haemochromatosis alleles in Egyptian patients with cirrhosis. Arab J Gastroenterol 2006; 7(2): 59-63.
  29.  Ahmad Settin, Mohammad Al-Haggar, Tarek El-Dosokey, Rizk Al-Baz, Nabil Abdelrazik, Manal Fouda, Salah Aref and Youseff Al-Tonbary. Prognostic cytogenetic markers in childhood acute lymphoblastic leukemias, Cases from Mansoura, Egypt. Haematology 2006 (October – December); 11(5, 6): 341-349.
  30.  Ahmad Settin, Mohammad Al-Haggar, Tarek El-Dosokey, Rizk Al-Baz, Nabil Abdelrazik, Manal Fouda, Salah Aref and Youseff Al-Tonbary. Prognostic cytogenetic markers in childhood acute lymphoblastic leukemias, Cases from Mansoura, Egypt. Hematology. 2007 April; 12(2): 103-111.
  31. Ahmad Settin, Mohammad Al-Haggar, Tarek El-Dosokey, Rizk Al-Baz, Nabil Abdelrazik, Manal Fouda, Salah Aref and Youseff Al-Tonbary. Prognostic cytogenetic markers in childhood acute lymphoblastic leukemias. Indian J Pediatr 2007 Mar; 74(3): 255-263.
  32.  Nabil Abdel-Razik, Mohammad Al-Haggar, Hala Al-Marsafawy, Hisham Abdel-Hadi, Rizk Al-Baz: Impact of long-term iron supplementation in breast-fed infants. Ind J Pediatr 2007; 74(8): 937-745.
  33. Mohammad Al-Haggar, Zakaria Al-Morsy, Sohier Yahia, Nehad Chalaby, Amany Ragab and Abeer Mesbah. Correlation of Thyroid and Growth Hormones to Chromosomal Instability in Egyptian Fanconi Anemia Patients.. Ind J Pediatr 2008; 75(7): 679-684.
  34. Mohamed Nezar, Azza Abd El-Baky, Othman Soliman, Ayman Hammad, Mohammad Al-Haggar. Endothelin-1 and leptin as markers of intrauterine growth restriction. Indian Journal of Pediatrics; in Press.
  35. Mohammad Al-Haggar, Ashraf Bakr, Toshihiro Tajima,  Kenji Fujieda, Ayman Hammad, Ahmad Darwish, Afaf Al-Said, Sohier Yahia, Othman Soliman, Dina Abdel-Hady: Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis: Unusual Clinical Associations and Novel Claudin16 Mutation in an Egyptian family. Clinical and Experimental Nephrology, In press, Published online January 24, 2009; DOI 10.1007/s10157-008-0126-6.
  36. Youssef Al-Tonbary, Mohammad Al-Haggar, Rasha EL-Ashry, Sahar EL-Dakroory, Hanan Azzam, Ashraf Fouda.Vitamin E and N-Acetylcysteine as Antioxidant Adjuvant Therapy in Children with Acute Lymphoblastic Leukemia. Advances in Hematology 2009; Article ID 689639, 5 pages, doi:10.1155/2009/689639.
  37. Mohammad Al-Haggar, Yahia S, Damjanovich K, Ahmad N, Hamada I, Bayrak-Toydemir P. p.R672C Mutation of MYH3 Gene in an Egyptian Infant Presented with Freeman-Sheldon Syndrome. Indian J Pediatr. 2010 Oct 6.
  38.  Mohammad Al-Haggar, Sohier Yahia, Dina Abdel-Hadi, Franz Grill, Ali Al Kaissi. Sirenomelia (symelia apus) with Potteri's syndrome in connection with gestational diabetes mellitus: A case report and literature review. African Health Sciences, vol. 10, no. 4, pp. 395–399, 2010.
  39. Mohammad Al-Haggar, Osamu Sakamoto, Ali Shaltout, Amany El-Hawary, YahyaWahba, and Dina Abdel-Hadi. Fanconi Bickel Syndrome: Novel mutations in GLUT 2 gene causing a distinguished form of renal tubular acidosis in two unrelated Egyptian families. Case Reports in Nephrology 2011, 5 pages. doi:10.1155/2011/754369.
  40. Mohammad Al-Haggar, Osamu Sakamoto, Ali Shaltout, Amany Al-Hawari, Yahya Wahba, Dina Abdel-Hadi. Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi-Bickel syndrome: revisited gene atlas for renumbering. Clin Exp Nephrol. 2012 Feb 18.
  41. Mohammad Al-Haggar M, Madej-Pilarczyk A, Kozlowski L, Bujnicki JM, Yahia S, Abdel-Hadi D, Shams A, Ahmad N, Hamed S, Puzianowska-Kuznicka M. A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome. Eur J Hum Genet. 2012 May 2. doi: 10.1038/ejhg.2012.77.
  42. El-Sayyad HI, Mohammad Al-Haggar, El-Ghawet HA, Bakr IH. Cardiomyopathy and angiogenesis defects of Wistar rat fetuses of diabetic and hypercholesterolemic mothers. Nutrition. 2012 Apr 20. Epub ahead of print.
  43. Mohammad Al-Haggar, Anna Taranta, Amany El-Hawary, Afaf Al-Said, Abdel-Aziz Shaban and Yahya Wahba. Novel truncating mutation in the CTNS gene in an Egyptian family with cases of infantile nephropathic cystinosis and congenital heart malformations. Middle East Journal of Medical Genetics 2012, 1:71–75.
  44.  Al-Tonbary Y, Mohammad Al-Haggar, Salama O, Abul-Kheir M, El-Alfy A, Hafez M. Platelet count and serum thrombopoietin level as predictors for morbidity and/or mortality in thrombocytopenic neonates. Hematology. 2012 Nov; 17(6):341-5. doi:10.1179/1607845412Y.0000000026. Epub 2012 Sep 12.
  45. Mohammad Al-Haggar, Ahmad N, Yahia S, Shams A, Hasaneen B, Hassan Hassan R, Wahba Y, Salem NA, Abdel-Hady D. Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature. Case Rep Genet. 2013; 2013:834605. doi: 10.1155/2013/834605. Epub 2013 Jan 23.
  46.  Mohammad Al-Haggar, Shams A, Madej-Pilarczyk A, Barakat T, Puzianowska-Kuznicka M. Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu LMNA mutation and in their asymptomatic heterozygotic mothers. J Clin Pathol. 2013 Jun 17. [Epub ahead of print]
  47. Mohammad Al-Haggar, Anna Taranta, Paola Bencivenga, Nermin Ahmad, Hany Abo Hadid and Yahya Wahba. A Recent Experience in an Egyptian Medical Center: Strategies for the Clinical and Genetic Diagnoses of Nephropathic Cystinosis. British Journal of Medicine & Medical Research 3(4): 1918-1928, 2013
  48. Mohammad Al-Haggar. Evolving Molecular Methods for Detection of Mutations (Review). Gene Technology2013, 2:1. http://dx.doi.org/10.4172/gnt.1000e104  
  49. Mohammad Al-Haggar, Balkis Khair-Allaha, Mohammad Islam and Abdalla Mohamed. Bioinformatics in High Throughput Sequencing: Application in Evolving Genetic Diseases (Review). J Data Mining Genomics Proteomics 2013, 4:3. http://dx.doi.org/10.4172/2153-0602.1000131
  50.  Mohammad Al-Haggar. Fanconi-Bickel syndrome as an example of marked allelic heterogeneity. World J Nephrol. 2012 Jun 6;1(3):63-8. doi: 10.5527/wjn.v1.i3.63.
  51.  Mohammad Al-Haggar. Cystinosis as a lysosomal storage disease with multiple mutant alleles: Phenotypic-genotypic correlations. World J Nephrol. 2013 Nov 6;2(4):94-102.
  52.  Mohammad Al-Haggar, Carlo R. Largiadèr, Dina Abdel-Hady, Tarik Barakat, Jean-Marc Nuoffer, Abdel-Aziz Al-Refaei. Partial expression of ornithine transcarbamylase deficiency in an Egyptian female carrier. International Journal of Gynaecology and Obstetrics, In Press, Corrected Proof, Available online 31 October 2013.
  53. El-Sayyad HI, Mohammad Al-Haggar, El-Ghawet HA, Bakr IH. Effect of maternal diabetes and hypercholesterolemia on fetal liver of albino Wistar rats. Nutrition. 2014 Mar;30(3):326-36. doi: 10.1016/j.nut.2013.08.016. PMID: 24484682.
  54. Mohammad Al-Haggar: SNPs as Co-morbid Factors for Drug Abuse and Ischemic Heart Disease. Gene Technology; 2014, 3:1, http://dx.doi.org/10.4172/2329-6682.1000107.
  55. Mohammad Al-Haggar, Yahia S, Abdel-Hady D, Al-Saied A, Al-Kenawy R, Abo-El-Kasem R. Phenotype-genotype updates from familial Mediterranean fever database registry of Mansoura University Children's Hospital. Indian J Hum Genet 05/2014; 20(1): 43-50.
  56. Mohammad Al-Haggar, Nanees Salem, Yahya Wahba, Nermin Ahmad, Laurence Jonard, Dina Abdel-Hady, Amany El-Hawary, Ashraf El-Sharkawy, Abdel-Rhman Eid, Amira El-Hawary. Novel homozygous SLC29A3 mutations among two unrelated Egyptian families with spectral features of H-syndrome. Pediatr Diabetes. 2014 Jun 4. doi: 10.1111/pedi.12160, Pages 1-12. PMID: 24894595
  57. Zedan M, Bakr A, Shouman B, Zaghloul H, Al-Haggar M, et al. (2014) Single Nucleotide Polymorphism of IL4C-590T and IL4RA 175V and Immunological Parameters in Egyptian Asthmatics with Different Clinical Phenotypes. J Allergy Ther 5: 189. doi:10.4172/2155-6121.1000189
  58. Bakr A, Al-Haggar M, Eid R, Wahba Y, Coucke P, Hafez M, et al., editors. Focal Segmental Glomerulosclerosis In A Child With Marfan Syndrome And Novel Fibrillin Gene Mutation. PEDIATRIC NEPHROLOGY; 2014: SPRINGER 233 SPRING ST, NEW YORK, NY 10013 USA.

 

Mohammad Al-Haggar

Professor

 

  • :+2-050-2310661, +2-01111-715-350
  • DEPARTMENTDepartment of pediatrics & neurogenetics
    Faculty of medicine,
    mansoura university, Mansoura
  • COUNTRYEgypt