nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
An audit of infants ‘unscreened’ by the neonatal screening system in Scotland during 1991
|
Tappin, David M. |
|
1995 |
|
4 |
p. 201-207 7 p. |
artikel |
2 |
Announcement
|
|
|
1992 |
|
4 |
p. 291-292 2 p. |
artikel |
3 |
Announcement
|
|
|
1993 |
|
4 |
p. 231- 1 p. |
artikel |
4 |
Assessing genetic risks — implications for health and social policy: response from the Newborn Screening Committee of the Council of Regional Networks for Genetic Services
|
Meaney, F.J. |
|
1996 |
|
4 |
p. 247-249 3 p. |
artikel |
5 |
Author index
|
|
|
1995 |
|
4 |
p. 225-226 2 p. |
artikel |
6 |
Author index of volume 1
|
|
|
1992 |
|
4 |
p. 293-295 3 p. |
artikel |
7 |
Author index of volume 2
|
|
|
1993 |
|
4 |
p. 233-234 2 p. |
artikel |
8 |
Commentary on neonatal mass-screening for congenital adrenal hyperplasia in Japan
|
Suwa, Seizo |
|
1993 |
|
4 |
p. 229-230 2 p. |
artikel |
9 |
Commentary on review by Sawada on screening for neuroblastoma in Japan
|
Brodeur, Garrett M. |
|
1992 |
|
4 |
p. 281-284 4 p. |
artikel |
10 |
Commentary on screening for neuroblastoma in Japan
|
Craft, A.W. |
|
1992 |
|
4 |
p. 285-287 3 p. |
artikel |
11 |
Contents of volume 3
|
|
|
1995 |
|
4 |
p. 229-231 3 p. |
artikel |
12 |
Contents of volume 1
|
|
|
1992 |
|
4 |
p. 297-299 3 p. |
artikel |
13 |
Contents of volume 2
|
|
|
1993 |
|
4 |
p. 237-239 3 p. |
artikel |
14 |
Description of quality assurance programs in newborn screening
|
Webster, Dianne |
|
1993 |
|
4 |
p. 219-228 10 p. |
artikel |
15 |
Erythrocyte uridine diphosphate galactose-4-epimerase deficiency identified by newborn screening for galactosemia in the United States
|
Ng, Won G. |
|
1993 |
|
4 |
p. 179-186 8 p. |
artikel |
16 |
Familial hypercholesterolemia in South Africa: to screen or not to screen? A national perspective
|
Hitzeroth, H.W. |
|
1996 |
|
4 |
p. 233-245 13 p. |
artikel |
17 |
Fragile X syndrome: examination of issues pertaining to population-based screening
|
Meadows, Kellen L. |
|
1996 |
|
4 |
p. 175-192 18 p. |
artikel |
18 |
Italian Society of Neonatal Screening
|
Cerone, R. |
|
1996 |
|
4 |
p. 255- 1 p. |
artikel |
19 |
Later manifestations of congenital hypothyroidism predicted by slightly elevated thyrotropin levels in neonatal screening
|
Harada, Shohei |
|
1995 |
|
4 |
p. 181-192 12 p. |
artikel |
20 |
Neonatal mass screening for biliary atresia
|
Matsui, Akira |
|
1993 |
|
4 |
p. 201-209 9 p. |
artikel |
21 |
Neonatal screening for congenital hypothyroidism: analysis of interlaboratory quality control
|
Dhondt, J.L. |
|
1993 |
|
4 |
p. 187-199 13 p. |
artikel |
22 |
Neonatal screening for congenital hypothyroidism in Saudi Arabia: results of screening the first 1 million newborns
|
Al-Jurayyan, Nasir A.M. |
|
1996 |
|
4 |
p. 213-220 8 p. |
artikel |
23 |
Neonatal screening for cystic fibrosis using blood trypsin with complementary meconium lactase: an advisable strategy for the population of southern Europe
|
Pederzini, F. |
|
1995 |
|
4 |
p. 173-179 7 p. |
artikel |
24 |
Neonatal screening for inborn errors of metabolism in Switzerland
|
Colombo, J.P. |
|
1992 |
|
4 |
p. 249-251 3 p. |
artikel |
25 |
Neonatal screening in the context of early discharge in Spain
|
Alonso-Fernandez, Jose R. |
|
1996 |
|
4 |
p. 251-253 3 p. |
artikel |
26 |
Neuropsychological assessment in congenital hypothyroid children: importance of timing of replacement therapy
|
Battisti, Paola |
|
1996 |
|
4 |
p. 221-232 12 p. |
artikel |
27 |
Obituary
|
Guthrie, Robert |
|
1992 |
|
4 |
p. 289-290 2 p. |
artikel |
28 |
Osteomyelitis as a complication of capillary blood collection for neonatal screening
|
Gjurić, G. |
|
1992 |
|
4 |
p. 243-247 5 p. |
artikel |
29 |
Phenylketonuria screening using the Quantase phenylalanine kit in combination with a microfilter system and the dye Tartrazine
|
Elvers, L.H. |
|
1995 |
|
4 |
p. 209-223 15 p. |
artikel |
30 |
Recovery of white blood cells from dried blood spots on Guthrie cards
|
Yourno, Joseph |
|
1993 |
|
4 |
p. 211-217 7 p. |
artikel |
31 |
Results of screening for phenylketonuria using a lower cutoff value in early collected specimens
|
Arnopp, John J. |
|
1995 |
|
4 |
p. 193-199 7 p. |
artikel |
32 |
Screening for neuroblastoma in infants: more questions than answers
|
Woods, William G. |
|
1992 |
|
4 |
p. 273-279 7 p. |
artikel |
33 |
Screening infants for neuroblastoma in Japan
|
Sawada, Tadashi |
|
1992 |
|
4 |
p. 253-272 20 p. |
artikel |
34 |
Subject index
|
|
|
1995 |
|
4 |
p. 227- 1 p. |
artikel |
35 |
Subject index of volume 1
|
|
|
1992 |
|
4 |
p. 296- 1 p. |
artikel |
36 |
Subject index of volume 2
|
|
|
1993 |
|
4 |
p. 235- 1 p. |
artikel |
37 |
The Task Force on Genetic Testing needs your help
|
Holtzman, Neil A. |
|
1996 |
|
4 |
p. 257- 1 p. |
artikel |
38 |
Urinary pregnanetriol-3-glucuronide excretion in neonates and the use of urinary pregnanetriol-3-glucuronide/creatinine ratio in differentiating 21-hydroxylase deficiency
|
Saisho, S. |
|
1996 |
|
4 |
p. 193-203 11 p. |
artikel |
39 |
Use of the Guthrie bacterial inhibition assay to monitor blood phenylalanine for dietary treatment of phenylketonuria
|
Rohr, Frances J. |
|
1996 |
|
4 |
p. 205-211 7 p. |
artikel |