听力与言语-语言病理学

行为科学

医学伦理学

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  • Pediatric teledermatology--a survey of current use.

    abstract::Demand for pediatric dermatologic care far exceeds the supply of pediatric dermatologists. Teledermatology has been proposed as a solution to improve access to care, however, data regarding teledermatology use for pediatric patients are lacking. Surveys assessing use and experience with teledermatology were administer...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2008.00624.x

    authors: Fieleke DR,Edison K,Dyer JA

    更新日期:2008-03-01 00:00:00

  • Adams-Oliver syndrome: a sporadic occurrence with minimal disease expression.

    abstract::Adams-Oliver syndrome is a congenital condition comprising congenital scalp defects and distal limb abnormalities. We report a child with the sporadic form of the disease who had minimal disease expression, illustrating the wide clinical spectrum of the syndrome. ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00598.x

    authors: Narang T,Kanwar AJ,Dogra S

    更新日期:2008-01-01 00:00:00

  • Phacomatosis pigmentokeratotica: a follow-up report documenting additional cutaneous and extracutaneous anomalies.

    abstract::This is a follow-up report on a boy with phacomatosis pigmentokeratotica. At the age of 10 years he had, in addition to a sebaceous nevus and a speckled lentiginous nevus, multiple lesions of a collagen nevus localized on the chin and in the lumbar area. On the left shoulder, a small telangiectatic spot was present wi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00588.x

    authors: Boente Mdel C,Asial RA,Happle R

    更新日期:2008-01-01 00:00:00

  • Congenital leukemia cutis.

    abstract::We describe a premature neonate who was born with pancytopenia and a single subcutaneous nodule on her right lower extremity. A biopsy specimen from the nodule demonstrated a dense infiltrate of pleomorphic mononuclear cells that extended throughout the dermis and into the subcutaneous tissue. Immunohistochemical stai...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00578.x

    authors: Fender AB,Gust A,Wang N,Scott GA,Mercurio MG

    更新日期:2008-01-01 00:00:00

  • Lymphangioma scroti.

    abstract::Lymphangiomas are congenital malformations of the lymphatic system. We report a 10-year-old boy with lymphatic malformation of the scrotum, which presented as a multiloculated scrotal mass associated with edema of the left thigh and left cryptorchidism. Histopathologic examination showed scrotal lymphangioma cavernosu...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00557.x

    authors: Vikicevic J,Milobratovic D,Vukadinovic V,Golubovic Z,Krstic Z

    更新日期:2007-11-01 00:00:00

  • Acanthosis nigricans: a common finding in overweight youth.

    abstract::We evaluated the prevalence of acanthosis nigricans among urban youth. Youth (7-17 years) at nine pediatric practices completed surveys on demographics and family history of diabetes and had weight and height measured. Acanthosis nigricans was scored and digital photography of the neck performed. A total of 618 youth ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00547.x

    authors: Brickman WJ,Binns HJ,Jovanovic BD,Kolesky S,Mancini AJ,Metzger BE,Pediatric Practice Research Group.

    更新日期:2007-11-01 00:00:00

  • Hypomelanosis of ito-whorled hyperpigmentation combination: a mirror image presentation.

    abstract::We hereby report a 2-year-old boy who presented with a peculiar combination of hyperpigmented and hypopigmented skin lesions along the lines of Blaschko, sharply demarcated at the midline, both on the anterior and posterior trunk. Although combinations of hyperpigmented and hypopigmented skin lesions distributed along...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00529.x

    authors: Thapa R,Dhar S,Malakar R,Chakrabartty S

    更新日期:2007-09-01 00:00:00

  • Epidermal nevus syndrome and didymosis aplasticosebacea.

    abstract::The epidermal nevus syndrome is a disease complex consisting of the association of an epidermal nevus with various developmental abnormalities of the skin, eyes, nervous, skeletal, cardiovascular, and urogenital systems. The epidermal nevi are classified according to their predominant component; nevus sebaceus (sebace...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00507.x

    authors: Demerdjieva Z,Kavaklieva S,Tsankov N

    更新日期:2007-09-01 00:00:00

  • Hidradenitis suppurativa (acne inversa): management of a recalcitrant disease.

    abstract::Hidradenitis suppurativa is a chronic relapsing disorder of follicular occlusion that is often recalcitrant to therapy. Topical and systemic antibiotics, hormonal therapies, oral retinoids, immunosuppressant agents, and surgical treatment are some of the therapeutic alternatives used for this often recalcitrant and fr...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,评审

    doi:10.1111/j.1525-1470.2007.00544.x

    authors: Lam J,Krakowski AC,Friedlander SF

    更新日期:2007-09-01 00:00:00

  • Benign fibrous histiocytoma with osteoclast-like giant cells in an infant.

    abstract::Benign fibrous histiocytoma is a common soft tissue tumor that usually occurs in adults and is relatively rare in childhood. This report describes a 7-month-old Caucasian boy with an enlarging firm congenital nodule on his occipital scalp. Histologic analysis revealed a benign fibrous histiocytoma with osteoclast-like...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00440.x

    authors: Stinehelfer SE,Woosley JT,Losken HW,Morrell DS

    更新日期:2007-09-01 00:00:00

  • Stevens-Johnson syndrome associated with brucella infection.

    abstract::Stevens-Johnson syndrome is a potentially fatal condition that manifests mainly on the skin and mucosal surfaces but also affects other vital organs. There are no report of Stevens-Johnson syndrome caused by brucella infection in the literature. In this article, a previously healthy boy, diagnosed as Stevens-Johnson s...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00472.x

    authors: Babayigit A,Olmez D,Uzuner N,Caglayan S,Kumral A,Asilsoy SK,Ozer E,Karaman O

    更新日期:2007-07-01 00:00:00

  • Congenital curved nail of the fourth toe--three different clinical presentations.

    abstract::A congenital curved nail of the fourth toe (NIM 219070) is a rare nail deformity with no other associated abnormalities. Three patients with this congenital anomaly are reported here. Radiologic examination in all three revealed distal symphalangism of the fourth toes bilaterally. The clinical manifestations in these ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00454.x

    authors: Lin YC,Wu YH,Scher RK

    更新日期:2007-07-01 00:00:00

  • Bronchiolitis obliterans: a rare chronic pulmonary complication associated with Stevens-Johnson syndrome.

    abstract::Pulmonary manifestations are well recognized during the acute phase of Stevens-Johnson syndrome but persistent pulmonary sequela is rarely reported. We report two boys with bronchiolitis obliterans following the acute phase of Stevens-Johnson syndrome and discuss the clinical picture and treatment of persistent pulmon...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00433.x

    authors: Bakirtas A,Harmanci K,Toyran M,Razi CH,Turktas I

    更新日期:2007-07-01 00:00:00

  • Mucocutaneous findings in 100 children with Down syndrome.

    abstract::Down syndrome is the most common chromosomal abnormality affecting numerous organs, including the skin. Our aim was to study mucocutaneous findings in this syndrome. To do so, 100 children with Down syndrome attending Schools for Children with Special Educational Needs and centers affiliated to the Welfare and Rehabil...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00412.x

    authors: Daneshpazhooh M,Nazemi TM,Bigdeloo L,Yoosefi M

    更新日期:2007-05-01 00:00:00

  • Prurigo pigmentosa associated with an atopic diathesis in a 13-year-old girl.

    abstract::We report an Italian prepubescent girl with the typical clinical and histologic features of prurigo pigmentosa associated with an atopic diathesis. The dermatitis disappeared after treatment with minocycline, leaving a brown, reticulated hyperpigmentation, with no recurrence. The association with an atopic diathesis c...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00402.x

    authors: Cota C,Donati P,Amantea A

    更新日期:2007-05-01 00:00:00

  • Mohs surgical treatment of a granular cell tumor on the toe of a child.

    abstract::Granular cell tumors are uncommon, usually benign tumors of neural origin. They are most often diagnosed in the third to sixth decades of life and are infrequently seen in the pediatric population. Although they can be found in a wide distribution throughout the body, more than half occur in the oral cavity and other ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00392.x

    authors: Abraham T,Jackson B,Davis L,Yu J,Peterson C

    更新日期:2007-05-01 00:00:00

  • Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin.

    abstract::We report a family affected to the fourth generation by uncombable hair syndrome. This syndrome is characterized by unruly, dry, blond hair with a tangled appearance. The family pedigree strongly supports the hypothesis of autosomal dominant inheritance; some members of the family had, apart from uncombable hair, mino...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00385.x

    authors: Boccaletti V,Zendri E,Giordano G,Gnetti L,De Panfilis G

    更新日期:2007-05-01 00:00:00

  • Cerebriform intradermal nevus.

    abstract::Cerebriform intradermal nevus is a rare form of cutis verticis gyrata. Clinically it manifests as a scalp deformity resembling the surface of the brain, with cerebriform morphologic characteristics. Degeneration into malignant melanoma has been reported. Herein, a cerebriform intradermal nevus of the scalp in a 7-year...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00361.x

    authors: Yazici AC,Ikizoglu G,Baz K,Polat A,Ustunsoy D

    更新日期:2007-03-01 00:00:00

  • Response to IL-1-receptor antagonist in a child with familial cold autoinflammatory syndrome.

    abstract::Familial cold auto-inflammatory syndrome, Muckle-Wells syndrome and chronic infantile neurologic, cutaneous, articular syndrome are related disorders associated with mutations in the CIAS1 gene. They appear to represent a continuum of one disease characterized by IL-1-mediated inflammation. Until recently, these condi...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00343.x

    authors: O'Connell SM,O'Regan GM,Bolger T,Hoffman HM,Cant A,Irvine AD,Watson RM

    更新日期:2007-01-01 00:00:00

  • Acquired ichthyosis as a manifestation of acute cutaneous graft-versus-host disease.

    abstract::Acquired ichythosis has been described in adult hematopoietic stem cell transplant recipients. While some authors have suggested the association of acquired ichythosis with cutaneous graft-versus-host disease, the evidence to support this association is rare. We describe a patient who developed enteritis secondary to ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00333.x

    authors: Huang J,Pol-Rodriguez M,Silvers D,Garzon MC

    更新日期:2007-01-01 00:00:00

  • Unnecessary milk elimination diets in children with atopic dermatitis.

    abstract::Milk elimination diets are frequently adopted in the treatment of atopic dermatitis, although the real prevalence of clinically relevant food allergy remains unclear and reports from different authors are often in disagreement. We investigated the percentage of children allergic to cow's milk compared with the rate of...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2007.00323.x

    authors: Sinagra JL,Bordignon V,Ferraro C,Cristaudo A,Di Rocco M,Amorosi B,Capitanio B

    更新日期:2007-01-01 00:00:00

  • Clinical resolution of a neonatally eroded giant congenital melanocytic nevus.

    abstract::We report an unusual occurrence of spontaneous pigmentary regression with a desmoplastic reaction in a neonatally eroded giant congenital melanocytic nevus. This process has been documented with photographs and skin biopsy specimens. Neonatal histology demonstrated connective tissue proliferation. Histology at age 5 y...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00311.x

    authors: Gass JK,Grant JW,Hall PN,Atherton DJ,Burrows NP

    更新日期:2006-11-01 00:00:00

  • Hypopigmented mycosis fungoides associated with atopy in two children.

    abstract::Mycosis fungoides is very rare in children. Hypopigmented lesions of this disease are usually observed in dark-skinned individuals and often show a T supressor CD8(+) phenotype. Two Caucasian children with predominantly hypopigmented lesions of mycosis fungoides are presented here. Atopy was a concomitant feature in b...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00291.x

    authors: Onsun N,Kural Y,Su O,Demirkesen C,Büyükbabani N

    更新日期:2006-09-01 00:00:00

  • Celiac disease presenting with chilblains in an adolescent girl.

    abstract::Chilblains, or pernio, are cutaneous lesions that may accompany systemic illnesses including states of malnutrition and autoimmune diseases. We report an adolescent girl in whom chilblains were the chief presenting sign of celiac disease. A gluten-free diet led to weight gain and resolution of the chilblains. We specu...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00281.x

    authors: St Clair NE,Kim CC,Semrin G,Woodward AL,Liang MG,Glickman JN,Leichtner AM,Binstadt BA

    更新日期:2006-09-01 00:00:00

  • Improvement of atopic dermatitis and reduction of skin allergic responses by oral intake of konjac ceramide.

    abstract::Although topical application of ceramide is effective in the treatment of atopic dermatitis, its effect is transient. Thus, the effect of oral intake of ceramide on atopic dermatitis was studied. Two groups of 25 children with moderate atopic dermatitis, who were allergic to house dust mite took either milk sugar (con...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00268.x

    authors: Kimata H

    更新日期:2006-07-01 00:00:00

  • Vitamin a deficiency phrynoderma associated with chronic giardiasis.

    abstract::Phrynoderma is a rare form of follicular hyperkeratosis associated with deficiencies in vitamins A or C or essential fatty acids. We report a 6-year-old boy with an unusual presentation of phrynoderma, characterized by multiple minute digitate hyperkeratoses associated with hair casts and related to a severe deficienc...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00261.x

    authors: Girard C,Dereure O,Blatière V,Guillot B,Bessis D

    更新日期:2006-07-01 00:00:00

  • Double-blind, randomized, placebo-controlled trial of the use of topical 10% potassium hydroxide solution in the treatment of molluscum contagiosum.

    abstract::Molluscum contagiosum is a common viral infection of the skin that frequently affects children. Lesions take between 6 and 18 months to resolve spontaneously and are a source of great embarrassment to both caretakers and children, often affecting attendance at school and limiting social activity. Treatment options to ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章,随机对照试验

    doi:10.1111/j.1525-1470.2006.00235.x

    authors: Short KA,Fuller LC,Higgins EM

    更新日期:2006-05-01 00:00:00

  • Cutaneous manifestations and massive genital involvement in Hennekam syndrome.

    abstract::We describe a 16-year-old boy with intestinal lymphangiectasia, lymphedema of the limbs and genitalia, mild mental retardation, and facial anomalies (Hennekam syndrome) and cutaneous lesions. Severe edema in the genital area created a gigantic mass that included the scrotum and penis. Numerous grouped red-violaceous p...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00225.x

    authors: Musumeci ML,Nasca MR,De Pasquale R,Schwartz RA,Micali G

    更新日期:2006-05-01 00:00:00

  • Growth, bone mineral accretion, and adrenal function in glucocorticoid-treated infants with hemangiomas-- a retrospective study.

    abstract::Hemangiomas, common proliferative vascular tumors, can grow rapidly in the first months of life. Although therapy with high-dose oral glucocorticoids is standard for lesions that threaten vital functions or are disfiguring, little is known about the endocrine consequences of this treatment. Using retrospective data, w...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00207.x

    authors: Lomenick JP,Backeljauw PF,Lucky AW

    更新日期:2006-03-01 00:00:00

  • Endemic pemphigus foliaceus in Venezuela: report of two children.

    abstract::Two native Yanomami children from the Venezuelan Amazonia with erythroderma were hospitalized on our service. Clinical, histologic, and immunofluorescence studies diagnosed endemic pemphigus foliaceous. Human leukocyte antigen class II showed DRB1*04 subtype *0411, which has not been previously associated with this di...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00197.x

    authors: González F,Sáenz AM,Cirocco A,Tacaronte IM,Fajardo JE,Calebotta A

    更新日期:2006-03-01 00:00:00

  • Cutaneous leishmaniasis: three children with Leishmania major successfully treated with itraconazole.

    abstract::We report the rare instance of four family members with numerous cutaneous lesions of Leishmania major contracted while on holiday in Algeria. Treatment was successful with oral itraconazole for the children and intralesional sodium stibogluconate for the mother. Cutaneous leishmaniasis should be considered in those w...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00177.x

    authors: White JM,Salisbury JR,Jones J,Higgins EM,Vega-Lopez F

    更新日期:2006-01-01 00:00:00

  • Transient aquagenic palmar hyperwrinkling: the first instance reported in a young boy.

    abstract::Transient reactive papulotranslucent acrokeratoderma is a rare palmoplantar keratoderma seen predominantly in adolescent and young adult women. Clinically it is characterized by translucent white papules generally involving the palmar surfaces after exposure to water. The typical "hands-in-the-bucket" sign, which is n...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2006.00168.x

    authors: Neri I,Bianchi F,Patrizi A

    更新日期:2006-01-01 00:00:00

  • Xanthoma disseminatum with hepatic involvement in a child.

    abstract::Xanthoma disseminatum is a rare, usually self-healing dermatologic disease of unknown etiology. Involvement of other organs and tissues including bone marrow, bone, and brain may be seen rarely in children. However, to date, hepatic involvement has not been reported. We describe a child with xanthoma disseminatum who ...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.00138.x

    authors: Büyükavci M,Selimoglu A,Yildirim U,Ertekin V,Atasoy M

    更新日期:2005-11-01 00:00:00

  • Clear-cell hidradenoma of the forearm in a young boy.

    abstract::We treated a 5-year-old boy with clear-cell hidradenoma of the forearm. Our literature search found only one previous report of this disease occurring during the first decade of life, and the present patient is the first with involvement of the limbs. This presentation demonstrates that clear-cell hidradenoma needs to...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.00115.x

    authors: Ozawa T,Fujiwara M,Nose K,Muraoka M

    更新日期:2005-09-01 00:00:00

  • Spectrum of phenotypic manifestations from a single point mutation of the p63 gene, including new cutaneous and immunologic findings.

    abstract::Mutations in the p63 gene have been identified in five human disorders characterized by varying degrees of limb anomalies, ectodermal dysplasia, and facial clefts. We report a new point mutation in the p63 gene in a family in which the mother was initially diagnosed with Rapp-Hodgkin syndrome and her two offspring man...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.00105.x

    authors: Steele JA,Hansen H,Arn P,Kwong PC

    更新日期:2005-09-01 00:00:00

  • Confluent and reticulated papillomatosis associated with tinea versicolor in three siblings.

    abstract::We describe three teenage siblings with confluent and reticulated papillomatosis, all presenting during a 6-month period. Two of the three patients had confirmed tinea versicolor, with positive potassium hydroxide scrapings, in association with this entity. This is the largest series of siblings with confluent and ret...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.22410.x

    authors: Stein JA,Shin HT,Chang MW

    更新日期:2005-07-01 00:00:00

  • Dramatic improvement of pyoderma gangrenosum with infliximab in a patient with PAPA syndrome.

    abstract::Infliximab, a chimeric antitumor necrosis factor alpha monoclonal antibody (anti-TNF alpha), has been recently shown to have a beneficial effect on pyoderma gangrenosum associated with inflammatory bowel disease. Patients with the syndromic triad of pyogenic sterile arthritis, pyoderma gangrenosum, and acne, an autoin...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.22320.x

    authors: Stichweh DS,Punaro M,Pascual V

    更新日期:2005-05-01 00:00:00

  • Calcinosis cutis following trauma.

    abstract::We report an 8-year-old boy who developed dystrophic calcinosis cutis that occurred following trauma. Multiple abrasions were observed in the inguinal folds after a soccer game. Subsequently, multiple papules with soft centers and white particles appeared in the same area. A biopsy specimen showed calcinosis cutis wit...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.22309.x

    authors: Larralde M,Giachetti A,Cáceres MR,Rodríguez M,Casas J

    更新日期:2005-05-01 00:00:00

  • A practical approach for the use of oral isotretinoin for infantile acne.

    abstract::Infantile acne is a rare occurrence. It is more common in boys and predominately occurs on the cheeks in infants between the ages of 1 and 16 months. Clinically, the lesions range from comedones to inflammatory papulopustules to cysts. Successful therapies include topical tretinoin, benzoyl peroxide and topical and or...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.22224.x

    authors: Barnes CJ,Eichenfield LF,Lee J,Cunningham BB

    更新日期:2005-03-01 00:00:00

  • Diffuse normolipemic plane xanthoma in a 9-year-old boy.

    abstract::Normolipemic plane xanthoma normally occurs in adults. We report the atypical instance of a 9-year-old boy who developed disseminated, flat, yellow-brown plaques up to 2 to 3 cm without any complaints. The histology showed the hallmarks of xanthoma, including the presence of CD68+ foam cells and Touton giant cells. No...

    journal_title:Pediatric dermatology

    pub_type: 杂志文章

    doi:10.1111/j.1525-1470.2005.22207.x

    authors: Hofmann M,Zappel K,Trefzer U,Audring H,Albrecht-Nebe H,Sterry W,Blume-Peytavi U

    更新日期:2005-03-01 00:00:00

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