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Determination of normal β values via radio frequency echo-tracking technique in a healthy Central European population

Clinical hemorheology and microcirculation, 2014, Vol.57 (2), p.185

2014

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Estimation of vessel age and early diagnose of atherosclerosis in progeria syndrome by using echo-tracking

Clinical hemorheology and microcirculation, 2010, Vol.44 (4), p.297

2010

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Combined Genetic Ablation of CD54 and CD58 in CAR Engineered Cytotoxic Lymphocytes Effectively Averts Allogeneic Immune Cell Rejection

BLOOD, 2022-11, Vol.140 (Supplement 1), p.1165-1166

2022

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Prognostic value of FDG-PET in Hodgkin lymphoma for posttreatment evaluation. Long term follow-up results

Neoplasma, 2010, Vol.57 (4), p.349

2010

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Size at birth in a rapidly developing economy: intrauterine growth pattern of UAE infants

Annals of human biology, 2008-01, Vol.35 (6), p.615-623

2008

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Novel genotype of mevalonic aciduria with fatalities in premature siblings

Archives of disease in childhood. Fetal and neonatal edition, 2004-01, Vol.89 (1), p.F90

2004

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Genetic Contribution to High Neonatally Lethal Malformation Rate in the United Arab Emirates

Community genetics, 2005-01, Vol.8 (1), p.31-34

2005

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Comparison of arterial stiffness parameters, epicardial fat volume and coronary calcium score in patients with coronary artery disease

European heart journal, 2013-08, Vol.34 (suppl 1), p.P1577-P1577

2013

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Gonococcal scalp abscess in a neonate delivered by caesarean section

Sexually transmitted infections, 1998-12, Vol.74 (6), p.451-451

1998

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CT and MR Patterns of Hypoxic Ischemic Brain Damage Following Perinatal Asphyxia

Journal of tropical pediatrics (1980), 2002-02, Vol.48 (1), p.5-9

2002

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Radiofrequency catheter ablation of left ventricular outflow tract tachycardia with the assistance of the CartoSound system

Europace (London, England), 2009-09, Vol.11 (9), p.1248-1249

2009

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Neonatal outcome in the United Arab Emirates: the effect of changes in resources and practices

Eastern Mediterranean health journal, 2005-07, Vol.11 (4), p.673-679

2005

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Pattern of central nervous system anomalies in a population with a high rate of consanguineous marriages

Clinical genetics, 1999-02, Vol.55 (2), p.95-102

1999

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Neonatal Schwartz-Jampel syndrome: a common autosomal recessive syndrome in the United Arab Emirates

Journal of medical genetics, 1996-03, Vol.33 (3), p.203-211

1996

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Neonatal audit in the United Arab Emirates: a country with a rapidly developing economy

Eastern Mediterranean health journal, 2000-01, Vol.6 (1), p.55-64

2000

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Complex consanguinity associated with short rib-polydactyly syndrome III and congenital infection-like syndrome: a diagnostic problem in dysmorphic syndromes

Journal of medical genetics, 1999-06, Vol.36 (6), p.461-466

1999

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INTRACARDIAC TUMOUR AND BRAIN LESIONS IN TUBEROUS SCLEROSIS: A case report of antenatal diagnosis by ultrasonography

Acta radiologica (1987), 2000-07, Vol.41 (4), p.371-374

2000

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Microlissencephaly

Pediatric neurology, 1998-04, Vol.18 (4), p.362-365

1998

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Intracardiac tumour and brain lesions in tuberous sclerosis : A case report of antenatal diagnosis by ultrasonography

Acta radiologica (1987), 2000-07, Vol.41 (4), p.371-374

2000

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Mediobasal and mantle defect of the prosencephalon: lobar holoprosencephaly, schizencephaly and diabetes insipidus

Neuropediatrics, 1998-10, Vol.29 (5), p.272

1998

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Further delineation of Nevo syndrome

Journal of medical genetics, 1997-05, Vol.34 (5), p.366-370

1997

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Birth prevalence and pattern of osteochondrodysplasias in an inbred high risk population

Birth defects research. A Clinical and molecular teratology, 2003-02, Vol.67 (2), p.125-132

2003

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ABVD chemotherapy of Hodgkin's disease

Neoplasma, 1997, Vol.44 (4), p.263

1997

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Larsen syndrome in siblings with consanguineous parents

Clinical dysmorphology, 1994-07, Vol.3 (3), p.263-265

1994

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Second malignancies after treatment for Hodgkin's disease

Leukemia & lymphoma, 2001-11, Vol.42 (6), p.1275-1281

2001

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Determination of normal β values via radio frequency echo-tracking technique in a healthy Central European population

Estimation of vessel age and early diagnose of atherosclerosis in progeria syndrome by using echo-tracking

Combined Genetic Ablation of CD54 and CD58 in CAR Engineered Cytotoxic Lymphocytes Effectively Averts Allogeneic Immune Cell Rejection

Prognostic value of FDG-PET in Hodgkin lymphoma for posttreatment evaluation. Long term follow-up results

Size at birth in a rapidly developing economy: intrauterine growth pattern of UAE infants

Novel genotype of mevalonic aciduria with fatalities in premature siblings

Genetic Contribution to High Neonatally Lethal Malformation Rate in the United Arab Emirates

Comparison of arterial stiffness parameters, epicardial fat volume and coronary calcium score in patients with coronary artery disease

Gonococcal scalp abscess in a neonate delivered by caesarean section

CT and MR Patterns of Hypoxic Ischemic Brain Damage Following Perinatal Asphyxia

Radiofrequency catheter ablation of left ventricular outflow tract tachycardia with the assistance of the CartoSound system

Neonatal outcome in the United Arab Emirates: the effect of changes in resources and practices

Pattern of central nervous system anomalies in a population with a high rate of consanguineous marriages

Neonatal Schwartz-Jampel syndrome: a common autosomal recessive syndrome in the United Arab Emirates

Neonatal audit in the United Arab Emirates: a country with a rapidly developing economy

Complex consanguinity associated with short rib-polydactyly syndrome III and congenital infection-like syndrome: a diagnostic problem in dysmorphic syndromes

INTRACARDIAC TUMOUR AND BRAIN LESIONS IN TUBEROUS SCLEROSIS: A case report of antenatal diagnosis by ultrasonography

Microlissencephaly

Intracardiac tumour and brain lesions in tuberous sclerosis : A case report of antenatal diagnosis by ultrasonography

Mediobasal and mantle defect of the prosencephalon: lobar holoprosencephaly, schizencephaly and diabetes insipidus

Further delineation of Nevo syndrome

Birth prevalence and pattern of osteochondrodysplasias in an inbred high risk population

ABVD chemotherapy of Hodgkin's disease

Larsen syndrome in siblings with consanguineous parents

Second malignancies after treatment for Hodgkin's disease

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