Results
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61.
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Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis. [electronic resource] by
- Pavone, P
- Pettoello-Mantovano, M
- Le Pira, A
- Giardino, I
- Pulvirenti, A
- Giugno, R
- Parano, E
- Polizzi, A
- Distefano, A
- Ferro, A
- Pavone, L
- Ruggieri, M
Producer: 20110808
In:
Neuropediatrics vol. 41
Availability: No items available.
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62.
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Fetal cells in maternal blood: a six-fold increase in women who have undergone amniocentesis and carry a fetus with Down syndrome: a multicenter study. [electronic resource] by
- Falcidia, E
- Parano, E
- Grillo, A
- Pavone, P
- Takabayashi, H
- Trifiletti, R R
- Scollo, P
- Dallapiccola, B
- Grammatico, P
- Novelli, A
- Paladini, D
- Monni, G
- Gulisano, A
- Scassellati, G
Producer: 20050310
In:
Neuropediatrics vol. 35
Availability: No items available.
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63.
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Pediatric autoimmune neuropsychiatric disorder associated with group a streptococcal infection: the role of surgical treatment. [electronic resource] by
- Pavone, P
- Rapisarda, V
- Serra, A
- Nicita, F
- Spalice, A
- Parano, E
- Rizzo, R
- Maiolino, L
- Di Mauro, P
- Vitaliti, G
- Coco, A
- Falsaperla, R
- Trifiletti, R R
- Cocuzza, S
Producer: 20141113
In:
International journal of immunopathology and pharmacology vol. 27
Availability: No items available.
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64.
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TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa. [electronic resource] by
- Banerjee, P
- Kleyn, P W
- Knowles, J A
- Lewis, C A
- Ross, B M
- Parano, E
- Kovats, S G
- Lee, J J
- Penchaszadeh, G K
- Ott, J
- Jacobson, S G
- Gilliam, T C
Producer: 19980224
In:
Nature genetics vol. 18
Availability: No items available.
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65.
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A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions. [electronic resource] by
- Carter, T A
- Bönnemann, C G
- Wang, C H
- Obici, S
- Parano, E
- De Fatima Bonaldo, M
- Ross, B M
- Penchaszadeh, G K
- Mackenzie, A
- Soares, M B
- Kunkel, L M
- Gilliam, T C
Producer: 19970827
In:
Human molecular genetics vol. 6
Availability: No items available.
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66.
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Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses. [electronic resource] by
- Shah, A B
- Chernov, I
- Zhang, H T
- Ross, B M
- Das, K
- Lutsenko, S
- Parano, E
- Pavone, L
- Evgrafov, O
- Ivanova-Smolenskaya, I A
- Annerén, G
- Westermark, K
- Urrutia, F H
- Penchaszadeh, G K
- Sternlieb, I
- Scheinberg, I H
- Gilliam, T C
- Petrukhin, K
Producer: 19971015
In:
American journal of human genetics vol. 61
Availability: No items available.
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