| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An executive functioning perspective in neurofibromatosis type 1: from ADHD and autism spectrum disorder to research domains
|
Smith, Taylor F.
|
|
|
36 |
10 |
p. 2321-2332
|
artikel
|
| 2 |
Ante-natal counseling in phacomatoses
|
Brabbing-Goldstein, Dana
|
|
|
36 |
10 |
p. 2269-2277
|
artikel
|
| 3 |
Clinical characterization of children and adolescents with NF1 microdeletions
|
Kehrer-Sawatzki, Hildegard
|
|
|
36 |
10 |
p. 2297-2310
|
artikel
|
| 4 |
Craniofacial bone alterations in patients with neurofibromatosis type 1
|
Chauvel-Picard, Julie
|
|
|
36 |
10 |
p. 2391-2399
|
artikel
|
| 5 |
Current status of MEK inhibitors in the treatment of plexiform neurofibromas
|
Gross, Andrea M.
|
|
|
36 |
10 |
p. 2443-2452
|
artikel
|
| 6 |
Current trends in the management of subependymal giant cell astrocytomas in tuberous sclerosis
|
Frassanito, Paolo
|
|
|
36 |
10 |
p. 2527-2536
|
artikel
|
| 7 |
Epilepsy in NF1: a systematic review of the literature
|
Bernardo, Pia
|
|
|
36 |
10 |
p. 2333-2350
|
artikel
|
| 8 |
Epilepsy surgery in tuberous sclerosis complex (TSC): emerging techniques and redefinition of treatment goals
|
Treiber, Jeffrey M.
|
|
|
36 |
10 |
p. 2519-2525
|
artikel
|
| 9 |
Genetic basis of neurofibromatosis type 1 and related conditions, including mosaicism
|
Legius, Eric
|
|
|
36 |
10 |
p. 2285-2295
|
artikel
|
| 10 |
Genetics of tuberous sclerosis complex: an update
|
Marom, Daphna
|
|
|
36 |
10 |
p. 2489-2496
|
artikel
|
| 11 |
Hemangioblastoma and von Hippel-Lindau disease: genetic background, spectrum of disease, and neurosurgical treatment
|
Klingler, Jan-Helge
|
|
|
36 |
10 |
p. 2537-2552
|
artikel
|
| 12 |
In memory of James Tait Goodrich
|
Abbott, Rick
|
|
|
36 |
10 |
p. 2195
|
artikel
|
| 13 |
Introduction to phacomatoses (neurocutaneous disorders) in childhood
|
Ruggieri, Martino
|
|
|
36 |
10 |
p. 2229-2268
|
artikel
|
| 14 |
I remember
|
Zerah, Michel
|
|
|
36 |
10 |
p. 2197
|
artikel
|
| 15 |
James Goodrich—as I knew him
|
Chatterjee, Sandip
|
|
|
36 |
10 |
p. 2209-2212
|
artikel
|
| 16 |
James Tait Goodrich 1946–2020
|
Mazza, Carlo
|
|
|
36 |
10 |
p. 2201-2206
|
artikel
|
| 17 |
James Tait Goodrich: a collector of friends
|
|
|
|
36 |
10 |
p. 2199-2200
|
artikel
|
| 18 |
James Tait Goodrich, MD, PhD. (4/16/1946–3/30/2020)
|
Keating, Robert F.
|
|
|
36 |
10 |
p. 2189-2191
|
artikel
|
| 19 |
James Tait Goodrich, MD, PhD
|
|
|
|
36 |
10 |
p. 2207-2208
|
artikel
|
| 20 |
James T. Goodrich, MD, PhD
|
Walker, Marion L. (Jack)
|
|
|
36 |
10 |
p. 2193-2194
|
artikel
|
| 21 |
Jim Tait Goodrich
|
Di Rocco, Concezio
|
|
|
36 |
10 |
p. 2187-2188
|
artikel
|
| 22 |
Management of spinal deformities and tibial pseudarthrosis in children with neurofibromatosis type 1 (NF-1)
|
Mladenov, Kiril V.
|
|
|
36 |
10 |
p. 2409-2425
|
artikel
|
| 23 |
Managing NF2-associated vestibular schwannomas in children and young adults: review of an institutional series regarding effects of surgery and bevacizumab on growth rates, tumor volume, and hearing quality
|
Gugel, Isabel
|
|
|
36 |
10 |
p. 2471-2480
|
artikel
|
| 24 |
Medical treatment of tuberous sclerosis-related epilepsy
|
Uliel-Sibony, Shimrit
|
|
|
36 |
10 |
p. 2511-2517
|
artikel
|
| 25 |
Neurocutaneous melanocytosis (melanosis)
|
Ruggieri, Martino
|
|
|
36 |
10 |
p. 2571-2596
|
artikel
|
| 26 |
Neurofibromatosis 1–associated optic pathway gliomas
|
Shofty, Ben
|
|
|
36 |
10 |
p. 2351-2361
|
artikel
|
| 27 |
Neurofibromatosis type 1–related hydrocephalus: causes and treatment considerations
|
Roth, Jonathan
|
|
|
36 |
10 |
p. 2385-2390
|
artikel
|
| 28 |
Neuroimaging in tuberous sclerosis complex
|
Russo, Camilla
|
|
|
36 |
10 |
p. 2497-2509
|
artikel
|
| 29 |
New treatment modalities in NF-related neuroglial tumors
|
Packer, Roger J.
|
|
|
36 |
10 |
p. 2377-2384
|
artikel
|
| 30 |
Options and strategies for hearing restoration in pediatric neurofibromatosis type 2
|
Mahboubi, Hossein
|
|
|
36 |
10 |
p. 2481-2487
|
artikel
|
| 31 |
Phacomatoses in the pediatric age group
|
Constantini, Shlomi
|
|
|
36 |
10 |
p. 2227-2228
|
artikel
|
| 32 |
Presenting symptoms in children with neurofibromatosis type 2
|
Gugel, Isabel
|
|
|
36 |
10 |
p. 2463-2470
|
artikel
|
| 33 |
Professor Wolfgang Wagner, the President of ISPN (2018–2019)
|
Wang, Kyu-Chang
|
|
|
36 |
10 |
p. 2213-2219
|
artikel
|
| 34 |
Role, function and challenges of multidisciplinary centres for rare diseases exemplified for neurofibromatosis type 1 syndrome
|
Toledano-Alhadef, Hagit
|
|
|
36 |
10 |
p. 2279-2284
|
artikel
|
| 35 |
Role of high-resolution ultrasound in detection and monitoring of peripheral nerve tumor burden in neurofibromatosis in children
|
Winter, Natalie
|
|
|
36 |
10 |
p. 2427-2432
|
artikel
|
| 36 |
Spinal manifestations of Neurofibromatosis type 1
|
Shofty, Ben
|
|
|
36 |
10 |
p. 2401-2408
|
artikel
|
| 37 |
Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons
|
Bianchi, Federico
|
|
|
36 |
10 |
p. 2553-2570
|
artikel
|
| 38 |
Surgical management of peripheral nerve sheath tumours in children, with special consideration of neurofibromatoses
|
Zipfel, Julian
|
|
|
36 |
10 |
p. 2433-2442
|
artikel
|
| 39 |
The value of screening tests in children with neurofibromatosis type 1 (NF1)
|
Baudou, Eloïse
|
|
|
36 |
10 |
p. 2311-2319
|
artikel
|
| 40 |
Treatment of malignant peripheral nerve sheath tumors in pediatric NF1 disease
|
Martin, Enrico
|
|
|
36 |
10 |
p. 2453-2462
|
artikel
|
| 41 |
Visual function tests including the role of optical coherence tomography in neurofibromatosis 1
|
Mezad-Koursh, Daphna
|
|
|
36 |
10 |
p. 2363-2375
|
artikel
|
| 42 |
Why are pediatric neurosurgeons not little adult neurosurgeons?
|
Wagner, Wolfgang
|
|
|
36 |
10 |
p. 2221-2225
|
artikel
|
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