| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A knock on the head is not a good thing: head injury and Alzheimer’s disease-like pathology
|
Snider, B.Joy
|
|
2000
|
6 |
1 |
p. 5-
1 p.
|
artikel
|
| 2 |
An animal model of attention deficit hyperactivity disorder
|
Gainetdinov, Raul R
|
|
2000
|
6 |
1 |
p. 43-44
2 p.
|
artikel
|
| 3 |
A schizophrenic mouse?
|
Evans, Kathryn L
|
|
2000
|
6 |
1 |
p. 5-
1 p.
|
artikel
|
| 4 |
Cancer research explosion imminent
|
Senior, Kathryn
|
|
2000
|
6 |
1 |
p. 2-3
2 p.
|
artikel
|
| 5 |
Cancer therapy: A2B adenosine antagonists for busting tumor angiogenesis?
|
Gurwitz, David
|
|
2000
|
6 |
1 |
p. 6-
1 p.
|
artikel
|
| 6 |
Causes and consequences of tumour acidity and implications for treatment
|
Stubbs, Marion
|
|
2000
|
6 |
1 |
p. 15-19
5 p.
|
artikel
|
| 7 |
DiGeorge syndrome: an enigma in mice and men
|
Srivastava, Deepak
|
|
2000
|
6 |
1 |
p. 13-14
2 p.
|
artikel
|
| 8 |
DiGeorge syndrome: complex pathogenesis? Maybe, maybe not
|
Baldini, Antonio
|
|
2000
|
6 |
1 |
p. 12-
1 p.
|
artikel
|
| 9 |
Dissecting the risk factors for pre-eclampsia
|
Habeck, Martina
|
|
2000
|
6 |
1 |
p. 4-
1 p.
|
artikel
|
| 10 |
Eotaxin and eosinophil recruitment: implications for human disease
|
Rankin, Sara M.
|
|
2000
|
6 |
1 |
p. 20-27
8 p.
|
artikel
|
| 11 |
FISHing for aneuploidies nets accurate results
|
Sansom, Clare
|
|
2000
|
6 |
1 |
p. 1-
1 p.
|
artikel
|
| 12 |
Individual haploinsufficient loci and the complex phenotype of DiGeorge syndrome
|
Novelli, Giuseppe
|
|
2000
|
6 |
1 |
p. 10-12
3 p.
|
artikel
|
| 13 |
Oral erythropoietin and prospects for maternal manipulation
|
Michie, Colin
|
|
2000
|
6 |
1 |
p. 6-
1 p.
|
artikel
|
| 14 |
PANDA identifies babies at risk of developing type 1 diabetes
|
Greener, Mark
|
|
2000
|
6 |
1 |
p. 3-
1 p.
|
artikel
|
| 15 |
Recent advances in understanding the molecular basis of primary congenital hypothyroidism
|
Macchia, Paolo E
|
|
2000
|
6 |
1 |
p. 36-42
7 p.
|
artikel
|
| 16 |
RNA viruses: emerging vectors for vaccination and gene therapy
|
Hewson, Roger
|
|
2000
|
6 |
1 |
p. 28-35
8 p.
|
artikel
|
| 17 |
The immune system versus cancer: can the immune system win?
|
Irvine, Alistair
|
|
2000
|
6 |
1 |
p. 7-9
3 p.
|
artikel
|
| 18 |
UFD1L is not the monogenic basis for heart defects associated with the CATCH phenotype* * We have recently revised the acronym CATCH22 to the CATCH phenotype to reflect unease at the ‘no win’ implication of the former label 4,5 . Retaining an all-encompassing acronym that stands for Cardiac Abnormality, T-cell deficits, Clefting and Hypocalcaemia can be defended because of the wide range of eponymous syndromes described in affected individuals. Some reflect the differing professional emphasis of those who provided the original reports; DiGeorge syndrome concentrates on the thymic and parathyroid hypoplasia while the Velocardiofacial syndrome reported by Shprintzen et al. took the craniofacial perspective. Takao et al. saw the phenotype from the cardiological angle with their Contruncal Anomaly Face syndrome while the lesser-known Strong syndrome was the first to emphasize the variable dominant disorder producing outflow tract, facial and psychiatric disturbance in different family members. Also included in the acronym are the less common and distinct phenotypes of Opitz G/BBB and Cayler asymmetric crying face syndrome, neither of which is exclusive to 22q11 deletion.
|
Goodship, Judith A.
|
|
2000
|
6 |
1 |
p. 14-
1 p.
|
artikel
|
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