戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 bryo, including impaired testicular descent (cryptorchidism).
2 y hypothyroidism, neurological symptoms, and cryptorchidism.
3 of left testicular hematoma and of the right cryptorchidism.
4 ge was referred for evaluation of left-sided cryptorchidism.
5 ng TDS-consistent effects of hypospadias and cryptorchidism.
6 hip seemed stronger for hypospadias than for cryptorchidism.
7 ce causes infertile bilateral intraabdominal cryptorchidism.
8 nt roles in male infertility associated with cryptorchidism.
9 dig cells, thereby providing a mechanism for cryptorchidism.
10 ster serum from the mothers of 217 sons with cryptorchidism, 197 sons with hypospadias, and 557 sons
11 re diagnosed with hypospadias and 6,878 with cryptorchidism (3,624 underwent corrective surgery).
12          Infertility is common, arising from cryptorchidism, anatomical malformations (such as epidid
13 naffected, male transheterozygotes displayed cryptorchidism and abnormal tortuosity of the ductus def
14 cking androgen action induce hypospadias and cryptorchidism and altered penile length in male rats, a
15 ll tumors (TGCTs) is poorly understood, with cryptorchidism and family history being the only well-es
16 sk indicators for the male genital anomalies cryptorchidism and hypospadias are prematurity and low b
17 s in singletons and twins and by patterns of cryptorchidism and hypospadias co-occurrence in individu
18                                              Cryptorchidism and hypospadias were associated with low
19           However, AGD in human infants with cryptorchidism and hypospadias, which are potential mani
20 etiologies of the male urogenital anomalies--cryptorchidism and hypospadias--are poorly understood.
21 icular dysgenesis syndrome disorders, namely cryptorchidism and hypospadias.
22 the association between placental weight and cryptorchidism and hypospadias.
23 e a significant increase in the incidence of cryptorchidism and micropenis.
24 as a candidate gene involved in hypospadias, cryptorchidism and other genitourinary (GU) tract anomal
25                                          For cryptorchidism and polythelia, the results were consiste
26 om undescended testes in boys with bilateral cryptorchidism and serving as a measure of testicular in
27 e, modulation of WNT4 expression in men with cryptorchidism and spermatogenic failure due to E2F1 cop
28 ted with genitourinary anomalies, especially cryptorchidism and/or hypospadias.
29  congenital nIHH (with micropenis, bilateral cryptorchidism, and absent puberty), a homozygous frames
30 ies, hypotonia, global developmental delays, cryptorchidism, and cardiac arrhythmias.
31  frequent include obesity, umbilical hernia, cryptorchidism, and congenital heart disease.
32 formations, short stature, pectus deformity, cryptorchidism, and developmental delay did not differ b
33 ing dysgenic testes, Leydig cell hypoplasia, cryptorchidism, and hypospadias.
34 actors related to race, estrogenic exposure, cryptorchidism, and infertility are becoming available.
35 es of sex development including hypospadias, cryptorchidism, and infertility.
36 s following the acute injury of experimental cryptorchidism, and were resistant to the chronic injury
37 peptide receptor 2, in cases of nonsyndromic cryptorchidism are infrequent and of unclear significanc
38 masculinization, resulting in hypospadias or cryptorchidism, are common, but their cause remains uncl
39                                              Cryptorchidism can result in infertility and increases r
40                Seven of 28 boys with WT with cryptorchidism carried WT1 mutations.
41  for Insl3 are viable, but exhibit bilateral cryptorchidism due to developmental abnormalities of the
42                         Risk factors include cryptorchidism, family history of testicular cancer, gon
43 owest decile (<10%) had higher risks of both cryptorchidism (hazard ratio = 1.52, 95% confidence inte
44 roteins may predispose to the development of cryptorchidism, hypospadias, and WTs.
45  tract abnormalities (including hypospadias, cryptorchidism, hypospermatogenesis, and testicular canc
46                            Increased risk of cryptorchidism in first-degree relatives suggests a sign
47  mutation, crsp, causing high intraabdominal cryptorchidism in homozygous males.
48  GREAT gene in the etiology in some cases of cryptorchidism in humans.
49 e temporal trends in human semen quality and cryptorchidism in infants have been associated with expo
50 lity and a concurrent increased incidence of cryptorchidism in male offspring (1995-2014).
51 s revealed genitourinary anomalies including cryptorchidism, incomplete separation of the hindgut fro
52 eletions and microduplications contribute to cryptorchidism, infertility and testicular tumors.
53  to be associated with testicular cancer are cryptorchidism, infertility, and overexposure to pestici
54 y presents during childhood with features of cryptorchidism, inguinal hernia or transverse testicular
55                             The incidence of cryptorchidism is estimated to be 2-4% or higher in some
56                                              Cryptorchidism is the most common form of disorder of se
57                                              Cryptorchidism is the most common urologic birth defect
58                 Impaired testicular descent (cryptorchidism) is one of the most frequent congenital a
59    In humans, failure of testicular descent (cryptorchidism) is one of the most frequent congenital m
60 nally, Crkl heterozygous adult males exhibit cryptorchidism, lower testis weight, lower sperm count,
61                Webbed neck, chest deformity, cryptorchidism, mental retardation and bleeding diathese
62 levels during pregnancy and adjusted odds of cryptorchidism (n = 219), hypospadias (n = 199), and pol
63                           Boys with isolated cryptorchidism (n = 71, age 13.4 +/- 5.8 months) or hypo
64 most common associated medical condition was cryptorchidism (nine of 83 patients, 11%).
65  completely repressed in the surgery-induced cryptorchidism of the rhesus monkey.
66           Male mice mutant for INSL3 exhibit cryptorchidism or defects in testis descent due to abnor
67 ns-nonachlor or oxychlordane level in either cryptorchidism or hypospadias (p-trend all > 0.45).
68      Our aim was to compare AGD in boys with cryptorchidism or hypospadias against normative data.
69                The quartile-specific ORs for cryptorchidism or hypospadias show no notable associatio
70  an association between chlordane levels and cryptorchidism or hypospadias.
71                                 Nonsyndromic cryptorchidism or undescended testis is a structural def
72  lysine 9 in histone H3, are associated with cryptorchidism (P = 0.0383).
73 gth were reduced in boys with hypospadias or cryptorchidism relative to normative data derived from a
74 er had testicular microcalcification and one cryptorchidism, risk factors for testicular germ-cell tu
75        The role of diagnostic laparoscopy in cryptorchidism seems well established, although attempts
76 ggests a significant genetic contribution to cryptorchidism susceptibility that may be modulated by e
77        Whereas the linkage of infertility to cryptorchidism, the failure of the testis to descend int
78 spite the high prevalence of hypospadias and cryptorchidism, the genetic basis for these conditions i
79 n with independent TGCT risk factors such as cryptorchidism, the PRS may guide screening decisions wi
80 trong predictors of the urogenital anomalies cryptorchidism (undescended testis) and hypospadias.
81  boys with masculinization disorders such as cryptorchidism, urethral defects and hypospadias.
82 GD and penile length SDS values in boys with cryptorchidism were longer than mean values in boys with
83                                    Boys with cryptorchidism were older (p = 0.048) compared with boys
84                                         With cryptorchidism, which is a common manifestation of PMDS,
85 igation revealed that E2f1-null mice develop cryptorchidism with severe gubernacular defects and prog
86 , oligozoospermia (18/181, 10%), and primary cryptorchidism with SPGF (26/155, 17%).