|
1.
Discrepancy between the splenic up take of 99 Tc m-
tin colloid and heat denatured 99 Tc m red blood cells in Sickle
cell disease- Nuclear Medicine Communication 6, 1985.
2.
The Role of Nuclear Medicine in diagnosis of Bony
and Splenic complications of Sickle Cell Disease, The Islamic World
Medical Journal 1986: 1: 19-21.
3.
Acute Lymphocytic Leukaemia in Children in
Kuwait, Journal of Kuwait Medical Assocation 1987 : 21: 307-314.
4.
Study of Renographic changes in children with Sickle
Cell Anaemia. Paper presented at Fourth Asia and Oceania Congress of
Nuclear Medicine- November 1988 Abstract No.P 53.
5.
Radionuclide
Imaging of the Spleen with Heat Denatured Technetium 99 m RBC when
the splenic reticuloendothelial system seems impaired. Journal of
Nuclear Medicine 1988 : 29: 320-323.
6.
Successful Pregnancies following remission in
childhood acute lymphoblastic leukaemia – case report. Annals of
Tropical Paediatrics 1991: 11: 301-303.
7.
Molecular characterization of alpha Thalassaemia
Determinants, B-Thalassaemia Allets and Bs Haplotypes
among Kuwaiti Arabs. The Journal of Acta Haematological 1994: 92:
176-181.
8.
Childhood Acute immune (idiopathic)
Thrombocytopaenic Purpura in Kuwait. The experience of
Al-Sabah Hospital. J Kuwait Medical Association 1996 : 28: 451-454.
9.
Endocrine disorders in B-Thalassaemia Major in
Kuwait. J Kuwait Medical Association 1996 : 28: 252-6.
10.
Diamond –
Blackfan Anaemia in Kuwait:
outcome of fourteen cases. J Kuwait Medical Association 1997 : 29:
269-274.
11.
Thalassaemia Major in Kuwait. J Trop Pediatr
1998: 44: 311-312.
12.
Childhood Chronic Immune Thrombocytopenic Purpura:
How far should we treat ? J Kuwait Medical Association 1998 :
30: 196-200.
13.
Trisomy 5 in Acute Lymphoblastic Leukaemia .Acta
Paediatr 2003 : 92 (7): 878-9.
14.
Homozygous Severe Protein C deficiency Type 1 :
Longterm Prophylactic intermittent therapy with subcutaneous
purified Protein C concentrate. First case report from
Kuwait. Kuwait Med J (In press)
15-Acyclovir induced reversible renal failure in an immunocompro
-mised child with extensive cutaneous herpes zoster. Kuwait Med J
(In press).
15.
Familial Diamond – Blackfan Anaemia. Case
report. J Trop Pediatr (In press).
NEUROLOGY UNIT PUBLICATIONS
1.
Besisso MS,
Neubauer D, Al-Rashied AA. Idiopathic torsion dystonia in two Arab
siblings. J Kuwait
Med Assoc 1987; 21, 30-42.
2.
Besisso MS,
Neubauer D, Al-Rashied AA, Hammouri MY. Subacute sclerosing
panencephalitis in children in
Kuwait. J
Kuwait Med Assoc
1988; 22, 53-74
3.
Neubauer D, Besisso MS, Al-Ajmi MO.
Childhood hemiplegia at Al-Sabah
Hospital Children’s Department between 1980-1989. J
Kuwait Med Assoc
1996; 28: 263-7
4.
Al-Othman NO, Neubauer D, Karaguiosov KL.
A case of tuberculous meningitis
complicated by multiple basal ganglia tuberculomas. J
Kuwait Medical Journal
1998; 30 (4); 351-353.
5.
Besisso MS,
Cindro L, Neubauer D, Trontelj JV, Al-Busairi S, Bushnak R,
Al-Mansoor S, Hammuri M, Al-Rashied AA, Ravnik I. Prognosis and risk
factors in febrile convulsions: A prospective study of 150 children
in Kuwait.
Neuroepidemiology
1990; 9, 78-87.
6.
Khuraibet AJ, Neubauer D, Noor KZ, Haleem MA, Trontelj JV.
A case of neonatal tetanus with
characteristic neurophysiological findings. Muscle Nerve
1998; 21: 971-2.
7.
Besisso MS,
Neubauer D, Cindro L, Trontelj JV, Al-Rashied AA, Al-Hammouri MY.
Subakutni sklerozirajoči panencefalitis pri otrocih v Kuvajtu.
Slov Pediatr 1995; 4: 6-11.
8.
Zeljič, V.,
Neubauer, D. Children with cerebral palsy in
Kuwait. Brain Dev 1998; 20
(6): 412
9.
Al-Ajmi MO, Abdulla JK, Neubauer
D. A case of merosin-negative congenital muscular dystrophy with
extensive white matter abnormalities and electroencephalographic
changes in a Syrian boy. J Med Liban. 2001; 49(3):173-8.
10.
Neubauer D.
Child Neurology from Slovenia
at Al-Sabah Children's Hospital in – 15 years of shared and mutual
experience. Kuwait Medical Journal 2002; 14; 35-7.
11.
Lada Cindro
Heberle, Jamila KI Abdulla, Asma A ALTawari, Najeeb AL Othman,
Zaidan AL Mazidi; Peroxisomal Disorders: Short review with four case
reports: Kuwait Medical Journal 2001, 33(4):348-352
12.
Asma A.AL
Tawari, Nadia AL Torki, Lada Cindro Heberle, Mohamed A. AL Ajmi,
Jamila E. Abdullah, Najeeb AL Othman, Mona M. AL Ajmi. Newly
described multiple congenital anomalies in
methyelenetetrahydrofolate reductase deficiency in Arab child Poster
FP-K-019. the 9th International Child Neurology Congress,
Beijing, Chima; September
20-25, 2002.
13.
Asma A.AL
Tawari, Yousef Habib, Lada cindro hebrle, Mohamed A. AL Ajmi,
Jamila E. Abdullah, Maliha Boloshi, Ali Moosa. Canavan
disease in Kuwait. Poster
FP-K-020. the 9th International Child Neurology Congress,
beijing, China; September
20-25, 2002.
14.
Al-Tawari A,
Cindro-Heberle L, Abdulla J, Ramadan D, Neubauer D. A family with a
rare disorder of tetrahydrofolate reductase deficency. Neurology
2001; (abstract)
15.
Al-Ajmi MO, Abdulla JK, Neubauer
D. A case of merosin-negative congenital muscular dystrophy with
extensive white matter abnormalities and electroencephalographic
changes in a Syrian boy. J Med Liban. 2001; 49(3):173-8.
16.
Al Tawari AA,
Ramadan DG, Neubauer D, Heberle LC, Al Awadi F.An early onset form
of methylenetetrahydrofolate reductase deficiency: a report of a
family from Kuwait. Brain Dev
2002; 24(5):304-9.
17.
Asma A. AL
Tawari, Lada Cindro Heberle, Jamila K Abdullah, Mohamed A. AL Ajmi,
Ahmed AL Awadi, Amira Dia, Clinical study of recurrent refractory
convulsive status epilepticus in infancy, Epilepsia 2003 (abstract –
in press)
|
