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1 n)-for paediatric patients with desmoid-type fibromatosis.
2 deficiency and maternally inherited gingival fibromatosis.
3 old boy suffering from an aggressive form of fibromatosis.
4 well tolerated in children with desmoid-type fibromatosis.
5  is the most common genetic form of gingival fibromatosis.
6 e for autosomal-dominant hereditary gingival fibromatosis.
7  of the underlying genetic basis of gingival fibromatosis.
8 autosomal dominant form of isolated gingival fibromatosis.
9 rential diagnosis of GIST, including desmoid fibromatosis (0 of 17) and Schwannoma (0 of 3), were imm
10     A syndromic association between gingival fibromatosis and a wide variety of other genetically inh
11      The patient was diagnosed with gingival fibromatosis and aggressive periodontitis based on the c
12 ns for understanding other forms of gingival fibromatosis and corrective gingival-tissue management.
13 d to the genetic disorders, juvenile hyaline fibromatosis, and infantile systemic hyalinosis.
14  pharmacologically induced forms of gingival fibromatosis are known.
15           Purpose Desmoid tumors (aggressive fibromatosis) arise from connective tissue cells or fibr
16 s is the first report of hereditary gingival fibromatosis associated with aggressive periodontitis.
17     We previously identified retroperitoneal fibromatosis-associated herpesvirus (RFHV) as a simian h
18     The complete sequence of retroperitoneal fibromatosis-associated herpesvirus Macaca nemestrina (R
19 ed macaque homologs of KSHV, retroperitoneal fibromatosis-associated herpesvirus-Macaca nemestrina (R
20 reatment-induced biologic changes in desmoid fibromatosis (DF) earlier than conventional response cri
21     Many women who present with desmoid-type fibromatosis (DF) have had a recent pregnancy.
22 erapies are used for refractory desmoid-type fibromatosis (DF), but occasionally cause severe side ef
23 ltiple subcutaneous nodular tumors, gingival fibromatosis, flexion contractures of the joints, and an
24 ries, patients (<25 years) with desmoid-type fibromatosis from 57 centres in eight countries were pro
25 tion of ERK signaling in hereditary gingival fibromatosis gingival fibroblasts that was associated wi
26                          Hereditary gingival fibromatosis (HGF) is a fibrotic enlargement of the ging
27                          HEREDITARY GINGIVAL FIBROMATOSIS (HGF) is a fibrotic enlargement of the ging
28                          Hereditary gingival fibromatosis (HGF) is a fibrotic gingival enlargement.
29                          Hereditary gingival fibromatosis (HGF) is a rare, autosomal dominant form of
30                          Hereditary gingival fibromatosis (HGF) is an uncommon genetic condition char
31   Although non-syndromic hereditary gingival fibromatosis (HGF) is genetically heterogeneous, etiolog
32                          Hereditary Gingival Fibromatosis (HGF) is the most common genetic form of gi
33                          Hereditary gingival fibromatosis (HGF) is the most common genetic form of gi
34 ced gingival overgrowth, hereditary gingival fibromatosis (HGF), and neurofibromatosis I (von Recklin
35 ost common genetic form, hereditary gingival fibromatosis (HGF), is usually transmitted as an autosom
36                                      Ovarian fibromatosis is a benign disease of the ovary that is ra
37                          Hereditary gingival fibromatosis is a rare, genetically inherited overgrowth
38                                      Desmoid fibromatosis is a rare, nonmetastatic neoplasm marked by
39                                              Fibromatosis is a very rare condition in general populat
40 ssociated with maternally inherited gingival fibromatosis is an allelic disorder with cardiac arrhyth
41             Eventual diagnosis of aggressive fibromatosis is based on histopathological examination.
42                                     Gingival fibromatosis is characterized by a slowly progressive be
43                The genetic basis of gingival fibromatosis is unknown.
44  heterodimer partner Maf (muscle aponeurosis fibromatosis) is sufficient and necessary for robust tra
45                             Juvenile hyaline fibromatosis (JHF) and infantile systemic hyalinosis (IS
46                             Juvenile hyaline fibromatosis (JHF) is an autosomal recessive condition c
47  lesions) and deep, also known as aggressive fibromatosis (large, rapid-growing lesions).
48  a dominant trait in the family and gingival fibromatosis might be of hereditary origin.
49 sidual ovarian tissue is specific to ovarian fibromatosis; on MRI, this results in marked hypointensi
50                                     The term fibromatosis or desmoid tumor refers to a group of benig
51  included 17 single-lesion extremity desmoid fibromatosis patients who underwent standard-of-care MRI
52                       Simian retroperitoneal fibromatosis (RF) is a vascular fibroproliferative neopl
53 ) were evaluated and diagnosed with gingival fibromatosis suggesting that this is a dominant trait in
54                 There are two main groups of fibromatosis: superficial (small, slow-growing lesions)
55 sue tumors: desmoid tumor (DT) or aggressive fibromatosis, tenosynovial giant cell tumor (TGCT) or di
56  is the most common genetic form of gingival fibromatosis that develops as a slowly progressive, beni
57 otrexate (Mtx) in children with desmoid-type fibromatosis that is recurrent or not amenable to treatm
58 ON: In paediatric patients with desmoid-type fibromatosis, the EpSSG conservative strategy did not co
59  SOS1 is responsible for hereditary gingival fibromatosis type 1, a benign overgrowth condition of th
60 ion of the sample, a diagnosis of aggressive fibromatosis was established.